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Efficacy of treadmill exercises on arterial blood oxygenation, oxygen consumption and walking distance in healthy elderly people: a controlled trial



Regular physical exercise and healthy lifestyle can improve aerobic power of the elderly, although lung capacity gradually deteriorates with age. The aims of the study are: a) to evaluate the therapeutic effect of a treadmill exercise program on arterial blood oxygenation (SaO2), maximum oxygen consumption (VO2max) and maximum walking distance (MWD) in healthy elderly people; b) to examine the outcome of the program at a supervised short-term and at an unsupervised long-term.


A prospective, not-randomized controlled intervention trial (NRCT) was conducted. Eighty participants were allocated into two homogeneous groups (training group, TG, n = 40; control group, CG, n = 40). Each group consisted of 20 men and 20 women. Pre-intervention measures of SaO2, VO2max and MWD were taken of each participant 1-week before the training program to establish the baseline. Also, during the training program, the participants were followed up at the 12, 30 and 48th week. The exercise program consisted of walking on a treadmill with fixed 0 % grade of inclination 3 times weekly for 48 weeks; the first 12 weeks were supervised and the remaining 36 weeks of the program were unsupervised. Participants in the control group were encouraged to walk twice a week during 45 min, and received standard recommendations for proper health.


Related to the baseline, the SaO2, VO2max, and MWD is greater in the intervention group at the 12th (p <.001), 30th (p <.001) and 48th week (p <.001). Compared with the control group, there was also a significant improvement of SaO2, VO2max, and MWD valuesin the intervention group (p <.001) at the 12th (p <.001), 30th (p <.001) and 48th week (p <.001). Supervised intervention shows greater improvement of SaO2, VO2max, and MWD values than in the unsupervised one.


These results show that performing moderate exercise, specifically walking 3 days a week, is highly recommended for healthy older people, improving aerobic power.

Trial registration

Current Controlled Trials ISRCTN12621097.

Peer Review reports


Although the risk of disease and disability increases with age, poor health is not an inevitable result of aging. A healthy lifestyle, which can be achieved by practicing regular physical activity, healthy diet and early detection of diseases, could slow the effects of age [1]. As long as the elderly population continues to increase, it will be essential for family physicians to keep in mind that sedentary patients have to practice physical exercises regularly [2].

Lung function deteriorates gradually with age [3]. A trend towards lower arterial oxygen saturation (SaO2) in the elderly suggests that the biological processes of aging in one or more systems are occurring [4]. Maximal oxygen consumption (VO2max) is considered as the criterion for measurement of the cardio-respiratory fitness [5]. Some important factors can have an influence on VO2max (e.g.: Age, sex, heredity, body composition, training status, mode of exercise and a number of diseases) [6]. Also aging is associated with a decrease in postural control, gait speed, stride length, the distance walked during the synchronized walking test and there is also an increase in the variability of the gait [7].

Deterioration of lung function could be linked to respiratory impairment, particularly developed as a consequence of smoking or airway infections [8, 9]. In the clinical practice, before attributing any pathological process as related to the decreased lung capacity, aging deterioration must be considered to explain the physiological decline [10].

Many studies have investigated the effect of training on elderly patients suffering from different types of chronic diseases [1114] or the effect of rehabilitation on elderly subjects after the sequel of certain diseases [1517], but few studies investigated the effect of exercise on healthy elderly people [1820].

The cardio-pulmonary exercise test, and the distance walked during the walking tests, has been noted to be useful in the individual prescription of pulmonary rehabilitation and oxygen supplementation [21]. The targeted heart rate for moderate intensity exercise may be considered to be between 40 and 60 % of heart rate reserve, as determined by the exercise test. This heart rate range can be used for the initial prescription of many types of dynamic exercise and can be increased to 85 % (high intensity) if tolerated [22].

Regular exercise provides great health benefits in older people, as well as in the case of younger adults. Despite this, over 75% of older adults are insufficiently active to take advantage of these health benefits [2]. Supervised exercise therapy has shown clinically and statistically significant differences in the improvement of maximal treadmill walking distance, compared to non-supervised exercise therapy regimens [23], and results are usually closely related to adherence to the program [24].

Some studies have investigated the effect of adherence to the exercise program [25, 26], but few of them have studied the degree of compliance of the experimental group, and the impact on the patient [27, 28]. Also, another point of interest is how long the sustained effect of an exercise program lasts.

The aims of this study are: a) to evaluate the therapeutic effect of a treadmill exercise program on arterial blood oxygenation (SaO2), maximum oxygen consumption (VO2max) and maximum walking distance (MWD) in healthy elderly people controlling the different factors that can influence the results; b) to examine the outcome of the program at a supervised short-term and at an unsupervised long-term. These issues are targeted to report empirical evidence of the importance of maintaining an active lifestyle to slow down the aging effects on health, which, therefore, will lead to greater quality of life in older people.



Eighty healthy elderly people, from 459 assessed for eligibility (see Flow Diagram, Fig. 1), were evaluated from the outpatient clinic of ENT & Ophthalmology in a General Hospital in Cairo, Egypt. Previously, 375 were excluded (261 not meeting inclusion criteria, 92 declined to participate, and 22 by others reasons). Eighty four patients were selected for allocation from October 2010 to January 2011, of which two in the intervention group and one in the control group were lost to follow-up. Additionally, one person in the control group was excluded due to missing data. During the conduct of the trial, participants were blinded to the treatment until the study ended. Inclusion criteria to participate in the study were as following; age varying between 60 and 70 years, non-smokers or former smokers for more than 5 years and good general health (without neuromuscular, orthopaedic, neurological or cardiopulmonary conditions). Therefore, exclusion criteria were neuromuscular, orthopaedic, neurological or cardio-pulmonary diseases. Also, we excluded patients with any chronic deficit that would prevent exercise, according to the protocol of Fletcher et al. [22]. After performing a complete medical history, participants were instructed about the procedure and signed an informed consent.

Fig. 1

Flow Diagram (according to Consort 2010 Flow Diagram model)

Chest X-rays and ECG were performed to exclude any underlying pathology before the intervention. A 12 Channels Electrocardiogram Biocare (ECG-8080) was utilized to evaluate ECG. Necessary anthropometric measures were recorded such as height and weight to calculate Body Mass Index (BMI) and were introduced into the software along with the demographic data of the participants (name, age and sex). Height and weight scale IPR-scale08 model was used for the measurement of height, weight and BMI calculation. At the same time, instructions were given to the subjects to avoid food intake for 2 h before the test, the measures taken for hygiene and comfort in clothing as well as in footwear and to avoid any unusual physical efforts at least 12 h before the test.

Adherence, defined as the completion of the protocol by the end of it, was 100 %.

Experimental protocol and outcomes measures

In order to test the effect of a treadmill exercise program on health outcomes of healthy elderly people, a prospective, not-randomized single-blinded controlled intervention trial (NRCT) was conducted. Participants were allocated into two homogeneous groups (training group, TG, n = 40; control group, CG, n = 40) by matched features (sex, age, weight and BMI) by the research team. Each group consisted of 20 men and 20 women. Pre-intervention measurements of SaO2, VO2max and MWD were taken from each participant 1 week before the training program started in order to establish the baseline. Also, during the training program, the participants were followed up at the 12, 30, and 48th week.

The study has been approved by the Ethics Committee of the Department of Morphological Sciences, School of Medicine, University of Córdoba.

Measurement of Oxygen saturation (SaO2). Pulse Oximeter CMS 50DL Finger Pulse Oximeter SaO2 was used to measure SaO2. It was measured 1 week prior training; pulse oximeter was utilized to measure SaO2 in the right index of each individual. Each individual had to rest for 2 min before the beginning of the measurement. After placing the sensor on the finger, we waited until a reading was displayed on the oximeter, then we waited for another 10–15 s to verify a steady signal, this is followed by recording SaO2 and pulse every 10 s. Six observations were recorded and their average was used as the individual’s SaO2 as in previous studies [21]. These measurements were taken in a specific cardiopulmonary test, regardless of the training sessions.

Measurement of Maximum Oxygen consumption (VO2max). A Cardiopulmonary Exercise Test unit (CPET) Zan 800, a gas analyser of O2 and CO2 was used for the measurement of VO2max. Before conducting the test, the humidity collector was cleaned, the connected tube was checked, and the triple V- valve sensor disinfected and the gas analyser calibrated. The heart rate and blood pressure were recorded in the relaxed sitting position for each subject of the group. The mask was fixed with straps and then the triple tube V was connected to the mask. Initially, metabolic parameters such as oxygen consumption, carbon dioxide production and heart rate at rest were measured every 3 min. These measurements were taken in a specific cardiopulmonary test, regardless of the training sessions.

Maximal Walking Distance (MWD). This data was obtained from the treadmill DKN Run Tech 2.5. MWD is displayed on the screen. MWD data at baseline was recorded from an exercise test, the same test displayed in the first period of training sessions (warming up phase of 5 min on the treadmill, 20 min of active phase, and cooling down phase for a period of 5 min). At the 12th, 30th and 48th week, MWD was recorded from the training session in the corresponding week.


Participants were incorporated in an exercise program of moderate intensity (walking on the treadmill) 3 times weekly for 48 weeks; the first 12 weeks were supervised and the remaining 36 weeks of the program were unsupervised. The duration of complete training sessions was of 30 min the first 3 weeks, 40 min the next 2 weeks, 50 min the next 2 weeks, and 60 min until the end of the program.

The intervention exercise protocol was applied based on the protocol of Naughton [29]. The exercise program consisted of walking on a treadmill with fixed 0 % grade of inclination. The exercise program consists of three phases, which are the followings: a) Warming up phase of 5 min on the treadmill; b) Active phase in which the speed of the treadmill is increased to achieve at least 60 % and not more than 70 % of the maximum heart rate (HR max) according to the protocol of Fletcher and collaborators [22]. The treadmill inclination is fixed at 0 % grade during the whole program, so the intensity of the exercise could be increased or decreased only by changing the speed of the treadmill. The active phase of exercise is 20 min for the first 3 weeks, 30 min for the next 2 weeks, 40 min for the followings 2 weeks and finally for 50 min until the end of the program; c) Cooling down phase for a period of 5 min which is achieved by reducing the speed gradually till reaching zero and until the heart rate returned almost to resting level.

A treadmill DKN Run Tech 2.5 with adjustable speed, inclination and timer, and a large LCD screen with 23 training programs and 3 users’ profiles was used. The screen displays simultaneously walking time and distance, speed, inclination, burned calories and heart rate. The treadmill has front and/or side rails to aid in subject stability. Also, a Pulsometer (HR) p610 Accurex Plus was utilized for monitoring of heart rate.

Participants in the control group were encouraged to walk twice a week during 45 min through enlightening the benefits of moderate physical activity on health, and received standard recommendations for proper health. A telephone follow-up of the adherence to recommended exercise guidelines was conducted weekly.

Data management and analysis

The collected data was revised, coded, tabulated and introduced to a PC using Statistical package for Social Science (SPSS 19 for Windows). Data was presented and suitable analysis was done according to the type of data obtained for each parameter. Mean and standard deviation were reported to describe quantitative variables.

Prior to the application of the statistical tests to study the effect of the exercise program, initial differences of groups in anthropometric characteristics, age and initial values of the response variables was analysed. Compliance of normality assumption (Shapiro-Wilk test) of these variables in both groups has been verified. When this assumption is violated, we applied the nonparametric Mann-Whitney. If not, t-test for independent samples was applied.

To test the effect of the intervention on SaO2, VO2 and MWD we applied a Partially Repeated Measures Analysis of Variance. The within factor was the time of measurement and the between factor was the intervention (TG vs CG). Multivariate Test for repeated effects of Time and Time X Group (Pillai’s Trace) was used to evaluate the appropriateness of the application of the multivariate approach; the Mauchly’s test was applied to test the spherical pattern of the covariance matrix. If violated, to test the significance of effects we used repeated testing Huynh-Feldt (HF), which is the least conservative in correcting the effects of the violation of the sphericity assumption. If the significance of the interaction is checked, we studied the trend of time in each group by Repeated Measures Analysis of Variance, multivariate approach. Tukey pairwise comparisons were used to test the differences between time measurements. To reduce sources of variability, the gender of the participants is a blocking factor accounting for treatment variability between both genders. To evaluate the effect size, the partial Eta squared coefficient and the Cohen’s d were used. The level of significance applied was 5 %.


Prior to the application of the tests to study the effect of the intervention, initial differences of groups by gender in anthropometric characteristics, age and initial values of the response variables was analysed. It is observed that there are no differences between groups in all variables before the intervention (Table 1).

Table 1 Comparison of anthropometric values and response variables at baseline

The effect of the interaction repeated Time by Group has been found statistically significant, indicating a treatment effect, showing that the values of SaO2, VO2max and MWD have a different trend in the intervention group and in the control group. The partial Eta squared coefficient indicates a high effect size of the interaction. Also, there has been a significant main effect for time and group (Table 2). The gender of the participants is a blocking factor accounting for treatment variability between males and females.

Table 2 Comparisons of SaO2, VO2max and MWD at Baseline, 12, 30 and 48 weeks, and mixed effect model to test the effect Time, Time*Group and Group

Once the significance of the interaction was checked, we studied the trend of time in each group. In the control group there is a significant time effect for SaO2 [F (3, 114) = 5.174, p = .002, η2 = .120], VO2max [F (3, 114) = 3.376, p = .021; η2 = 0.082], and MWD [F (1.98, 75.09) = 7.778, p = .001; η2 = 0.170]. Tukey pairwise comparisons (Table 3) indicate that SaO2 is higher at 30 weeks than in the baseline and 48 weeks (Fig. 2). For VO2max, at 30 weeks a greater VO2max than at 48 weeks was found. Regarding MWD, pairwise comparisons (Table 3) indicate that it is lower at baseline than at 12, 30 and 48 weeks. A greater MWD was observed at 30 weeks than at 48 weeks.

Table 3 Pairwise comparisons by time at control and intervention groups (positive signs indicate an improvement)
Fig. 2

Interaction of group with time for SaO2 (Note that the y-axis does not intersect the x-axis at 0). Error bars represent standard deviation

The intervention group, as expected, showed a significant effect of the time (HF correction) for SaO2 [F (2.25, 85.61) = 55.165, p <.001; η2 = 0.592], VO2max [F (2.25, 85.61) = 55.165, p <.001; η2 = 0.592], and MWD [F (2.38, 90.58) = 87.806, p <.001; η2 = 0.698]. Pairwise comparisons (Table 3) show an increase in SaO2, VO2max and MWD from baseline to 12, 30 and 48 weeks. Highest SaO2, VO2max and MWD is observed at 12 weeks, descending at 30 and 48 weeks, showing that supervised exercise produces better outcomes that unsupervised exercise (Figs. 2, 3 and 4). At 30 and 48 weeks, SaO2, VO2max and MWD are similar, showing maintained intervention effects at the unsupervised period. All participants in both, intervention and control group, completed the corresponding exercise protocol, thus specific measurements of compliance were not registered.

Concerning the differences between groups at each time, there was no difference in SaO2, VO2max and MWD between the two groups in the pretest. All three measurements are higher in the intervention group at 12, 30 and 48 weeks (Table 2, Figs. 2, 3 and 4).

Fig. 3

Interaction of group with time for VO2max (Note that the y-axis does not intersect the x-axis at 0). Error bars represent standard deviation

Fig. 4

Interaction of group with time for MWD (Note that the y-axis does not intersect the x-axis at 0). Error bars represent standard deviation


The objective of the current intervention study was to evaluate the therapeutic efficacy of treadmill exercises on SaO2, VO2max and MWD in elderly healthy subjects. The results of this study show: a) that treadmill exercise produces a beneficial effect on these parameters in healthy elderly people; and b) that supervised exercises has better results than unsupervised exercise.

Intervention effects on pulmonary outputs (SaO2, VO2max and MWD)

We investigated the effect of controlled exercise (first aspect) on a treadmill (second aspect) in some parameters of routine clinical use. We meant to evaluate how programmed physical exercise can affect the physiological status of the elderly, improving their cardiopulmonary health, without including their quality of life. This was achieved by monitoring the physical activity and using objective data.

After the first 12 weeks of training (the controlled short-term program) there was a highly significant increase of the three variables of the study in the intervention group comparing it before and after the exercise program as well as with the control group. The physiological explanation is obvious because dealing with healthy elderly people who have made a controlled physical activity which dramatically improved the three variables of the study and the results have been highly positive. The control group also achieved an improvement in pulmonary outputs, but smaller than that from the intervention group. Thus, greater results in the intervention group could be related to the fact that both exercise programs were not dose-match, which, in turn, could lead to better achievement in the greater dose group. But this is not perceived as a limitation since we aim to compare a well-planned exercise program with standard recommendations for moderate physical activity in elderly people. Also, a highly significant improvement appears in the data at 30 and 48 weeks in the group that has complied with the unsupervised long term program, as compared with the control group.

The physical and physiological benefits achieved and the results showed match those given by Figoni et al. [30], whose relatively recent study found that after a training exercise program for 3 months, also with treadmills, and elderly people (mean age 69 years), an improvement was shown in both walking distance, and in arterial oxygen saturation. Also, Kalapotharakos, [31] following an aerobic training program, showed that there was an increase from 6.6 to 30 % VO2max in seniors. And, taking into account the study published by Wong et al. [32], every minute of normal gait increased per day leads to an increase in VO2max by 0.096 ml/kg/min. Even years ago, Shephard [33], showed that prolonged aerobic physical activity can reverse the decline in VO2max recovering and, consequently, the corresponding metabolic equivalent can increase in young moderately active subjects from 12 METs to18-24 METs by performing aerobic training such as distance running [22].

Meanwhile, Huang et al. [34] found that there was no change in SaO2 in a group of 16 women, whose ages ranged from 80 to 93 years, who participated in an exercise training program for 4 months. In the article it is unclear whether the lack of samples gave no significant statistical values or other factors influenced the study such as the advanced age of the group or even the type of training intervention.

These findings highlight that participation of older adults in aerobic exercise programs significantly improves cardiopulmonary response [31]. Treadmill walking may bring important health benefits in term of improvement in physical performance, fitness and its implications for the prevention of physical disability in older adults. This also reinforces the theory that low-to moderate intensity activities may improve cardio-respiratory fitness [32].

Supervised vs Unsupervised exercise effects

Bendermacher et al. [23], demonstrated the existence of significant differences and obvious clinical differences, when after a supervised exercise regimen, subjects improved distance walked on the treadmill compared with the unsupervised training for 3 months, still, the overall effect size of 0.59 (95 % confidence interval 0.31 to 0.85), the improvement resulted in a difference of about 150 m. In addition, the improved results in increasing the walking ability are maintained after the end of the program. As in our study, this study clearly shows greater improvement in cardiopulmonary outputs in response to supervised exercise program in healthy elderly. We have found that a supervised period of exercise program is related to better results in SaO2, VO2max and MWD values.

A previous study found a positive relationship between compliance and feedback [35]. Patients whose compliance were monitored and fed back on its developments and progress had more compliance than patients without supervision. This coincides substantially with the results exposed. Also, a few years ago, it was shown that compliance is reduced from 59 % in a supervised program to 29 % after 6 months of unsupervised exercise, concluding that patient compliance with physical therapy is unsatisfactory but monitoring improves adherence [36]. In our study, compliance, measured as the proportion of participants completing the exercise protocol in both the intervention and control group, was 100 %. This is a significant strength of the study, since achievement of adherence to an exercise program for nearly 1 year is a great achievement, showing that prescription of moderate exercise is well accepted in healthy elderly people. However, results showed that the supervised period of the intervention achieved greater improvement in pulmonary outputs, which could be related to motivation or compliance with instructions and encouragement from monitoring.


Limitations such as the small sample size could affect the validity of the results [37]. Our study included only 80 elderly healthy subjects. It was too difficult to identify more subjects between 60 and 70 years old without any chronic diseases who accepted to participate in a follow up study for nearly 1 year.

Another possible limitation was each participant’s psychological status at the time of exercise and his or her compliance to the supervised program. Motivation is an essential construct related to engagement in sustained physical activities [38], so the lack of motivation could lead to diminished compliance of the exercise program instructions. Although these limitations could not be avoided, our findings strongly suggest that exercise training programmes on a treadmill (short or long-term) can improve VO2max, SaO2 and maximum walking distance in elderly healthy subjects and the health benefits of the 3 parameters are closely related to the fitness of the subjects to the exercise program parameters, as showed in the supervised period of the intervention.

The purpose of this study was to investigate the effect of exercise and activity in older people in the Republic of Egypt considering that while in other nations and cultures these types of studies are quite frequent and started to be applied, in Egypt it is not so common because the average life expectancy and general health condition of the population is much lower than in Europe, and the practice of physical activity in old age is far from being an established plan. Consequently, it was difficult precisely at this time where the activity took place to do similar studies, the results had to be contrasted and their explanations had to be found.


The results of this study suggest that it is highly recommended for healthy older people to perform moderate exercise, specifically walking several days a week. Indicators of pulmonary capacity of the elderly (SaO2, VO2max and MWD) have improved from the practice of moderate exercise. Primary care physicians should consider this and other studies and strongly recommend older people living habits that include moderate physical activity in the ordinary way. Our findings were consistent and coherent, strongly indicating the external validity of the study.


12 W:

12 weeks

30 W:

30 weeks

48 W:

48 weeks




body mass index


control group


confidence interval 95 %


Cohen’s effect size


degrees of freedom


Huynh-Feldt test


maximum walking distance


group size


non-randomized controlled trial


significance level


t-test for independent samples


training group


arterial blood oxygenation


standard deviation


maximum oxygen consumption

η2 :

partial eta-squared


  1. 1.

    Kravitz L. Senior fitness research roundup. IDEA Fitness Journal. 2010;7(2):30–7.

    Google Scholar 

  2. 2.

    Nied RJ, Franklin B. Promoting and prescribing exercise for the elderly. Am Fam Physician. 2002;65(3):419–26.

    PubMed  Google Scholar 

  3. 3.

    Meyer KC. The role of immunity and inflammation in lung senescence and susceptibility to infection in the elderly. Semin Respir Crit Care Med. 2010;31(5):561–74. doi:10.1055/s-0030-1265897.

    Article  PubMed  Google Scholar 

  4. 4.

    Beall CM. Oxygen saturation increases during childhood and decreases during adulthood among high altitude native Tibetians residing at 3,800-4,200 m. High Alt Med Biol. 2000;1(1):25–32. doi:10.1089/152702900320658.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Laukkanen R. Development and evaluation of a 2-km walking test for assessing maximal aerobic power of adults in field conditions. Kuopio: University of Kuopio; 1993.

    Google Scholar 

  6. 6.

    Shephard RJ. Maximal oxygen intake and independence in old age. Br J Sports Med. 2009;43(5):342–6. doi:10.1136/bjsm.2007.044800.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Harris MH, Holden MK, Cahalin LP, Fitzpatrick D, Lowe S, Canavan PK. Gait in older adults: a review of the literature with an emphasis toward achieving favorable clinical outcomes, part II. Clin Geriatr. 2008;16(8):37–45.

    Google Scholar 

  8. 8.

    Ely EW, Wheeler AP, Thompson BT, Ancukiewicz M, Steinberg KP, Bernard GR. Recovery rate and prognosis in older persons who develop acute lung injury and the acute respiratory distress syndrome. Ann Intern Med. 2002;136:25–36.

    PubMed  Google Scholar 

  9. 9.

    Fry AM, Shay DK, Holman RC, Curns AT, Anderson LJ. Trends in hospitalizations for pneumonia among persons aged 65 years or older in the United States, 1988–2002. JAMA. 2005;294(21):2712–9.

    CAS  Article  PubMed  Google Scholar 

  10. 10.

    Fragoso CAV, Gill TM. Respiratory Impairment and the Aging Lung: a novel paradigm for assessing pulmonary function. J Gerontol A Biol Sci Med Sci. 2012;67A(3):264–75.

    Article  Google Scholar 

  11. 11.

    Kamahara K, Homma T, Naito A, Matsumura T, Nakayama M, Sekizawa K, et al. Circuit training for elderly patients with chronic obstructive pulmonary disease: a preliminary study. Arch Gerontol Geriatr. 2004;39(2):103–10.

    Article  PubMed  Google Scholar 

  12. 12.

    Austin J, Williams R, Ross L, Moseley L, Hutchison S. Randomised controlled trial of cardiac rehabilitation in elderly patients with heart failure. Eur J Heart Fail. 2005;7(3):411–7.

    Article  PubMed  Google Scholar 

  13. 13.

    Kyung KA, Chin PA. The effect of a pulmonary rehabilitation programme on older patients with chronic pulmonary disease. J Clin Nurs. 2008;17:118–25.

    Article  PubMed  Google Scholar 

  14. 14.

    Martins R, Neves A, Coelho-Silva M, Veríssimo M, Teixeira A. The effect of aerobic versus strength-based training on high-sensitivity C-reactive protein in older adults. Eur J Appl Physiol. 2010;110(1):161–9. doi:10.1007/s00421-010-1488-5.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Macchi C, Polcaro P, Cecchi F, Zipoli R, Sofi F, Molino-Lova R, et al. One-year adherence to exercise in elderly patients receiving postacute inpatient rehabilitation after cardiac surgery. Am J Phys Med Rehabil. 2009;88(9):727–34. doi:10.1097/PHM.0b013e3181b332a1.

    Article  PubMed  Google Scholar 

  16. 16.

    Giallauria F, Lucci R, Pietrosante M, Gargiulo G, De Lorenzo A, Vigorito C, et al. Exercise-based cardiac rehabilitation improves heart rate recovery in elderly patients after acute myocardial infarction. J Gerontol A Biol Sci Med Sci. 2006;61A(7):713–7.

    Article  Google Scholar 

  17. 17.

    Carinci F, Roti L, Francesconi P, Gini R, Tediosi F, Di Iorio T, et al. The impact of different rehabilitation strategies after major events in the elderly: the case of stroke and hip fracture in the Tuscany region. BMC Health Serv Res. 2007;7:95.

    Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Ferrari R, Kruel L, Cadore E, Alberton C, Izquierdo M, Umpierre D, et al. Efficiency of twice weekly concurrent training in trained elderly men. Exp Gerontol. 2013;48(11):1236–42. doi:10.1016/j.exger.2013.07.016.

    Article  PubMed  Google Scholar 

  19. 19.

    Leenders M, Verdijk L, van der Hoeven L, van Kranenburg J, Nilwik R, van Loon L. Elderly men and women benefit equally from prolonged resistance-type exercise training. J Gerontol A Biol Sci Med Sci. 2013;68(7):769–79. doi:10.1093/gerona/gls241.

    Article  PubMed  Google Scholar 

  20. 20.

    Sousa N, Mendes R, Abrantes C, Sampaio J, Oliveira J. Long-term effects of aerobic training versus combined aerobic and resistance training in modifying cardiovascular disease risk factors in healthy elderly men. Geriatr Gerontol Int. 2013;13(4):928–35. doi:10.1111/ggi.12033.

    Article  PubMed  Google Scholar 

  21. 21.

    Task Force ERS, Palange P, Ward SA, Carlsen KH, Casaburi R, Gallagher CG, et al. Recommendations on the use of exercise testing in clinical practice. Eur Respir J. 2007;29(1):185–209.

    Google Scholar 

  22. 22.

    Fletcher GF, Balady GJ, Amsterdam EA, Chaitman B, Eckel R, Fleg J, et al. Exercise standards for testing and training: a statement for healthcare professionals from the American Heart Association. Circulation. 2001;104:1694–740.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Bendermacher BL, Willigendael EM, Teijink JA, Prins MH. Supervised exercise therapy versus non-supervised exercise therapy for intermittent claudication. Cochrane Database Syst Rev. 2006;19(2):CD005263.

    Google Scholar 

  24. 24.

    Ringbaek T, Brondum E, Martinez G, Thogersen J, Lange P. Long-term effects of 1-year maintenance training on physical functioning and health status in patients with COPD: a randomized controlled study. J Cardiopulm Rehabil Prev. 2010;30(1):47–52. doi:10.1097/HCR.0b013e3181c9c985.

    Article  PubMed  Google Scholar 

  25. 25.

    Kozu R, Senjyu H, Jenkins S, Mukae H, Sakamoto N, Kohno S. Differences in response to pulmonary rehabilitation in idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease. Respiration. 2011;81(3):196–205. doi:10.1159/000315475.

    Article  PubMed  Google Scholar 

  26. 26.

    Maltais F, Bourbeau J, Shapiro S, Lacasse Y, Perrault H, Bernard S, et al. Effects of home-based pulmonary rehabilitation in patients with chronic obstructive pulmonary disease: a randomized controlled trial. Ann Intern Med. 2008;149(12):869–78.

    Article  PubMed  Google Scholar 

  27. 27.

    Bauldoff G, Hoffman L, Zullo T, Sciurba F. Exercise maintenance following pulmonary rehabilitation: effect of distractive stimuli. Chest. 2002;122(3):948–54.

    Article  PubMed  Google Scholar 

  28. 28.

    Steele B, Belza B, Cain K, Coppersmith J, Lakshminarayan S, Haselkorn J, et al. A randomized clinical trial of an activity and exercise adherence intervention in chronic pulmonary disease. Arch Phys Med Rehabil. 2008;89(3):404–12. doi:10.1016/j.apmr.2007.11.003.

    Article  PubMed  Google Scholar 

  29. 29.

    Naughton J, Balke B, Nagle F. Refinements in method of evaluation and physical conditioning before and after myocardial infarction. Am J Cardiol. 1964;14:837–43.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Figoni SF, Kunkel CF, Scremin AM, Asher A, Banks NL, Rivera A. Effects training on calf tissue oxygenation in men with intermittent claudication. PM R. 2009;1(10):932–40. doi:10.1016/j.pmrj.2009.08.453.

    Article  PubMed  Google Scholar 

  31. 31.

    Kalapotharakos VI. Aerobic exercise in older adults: effects on VO2 max and functional performance. Crit Rev Phys Rehabil Med. 2007;19:213–25. doi:10.1615/CritRevPhysRehabilMed.v19.i3.30.

    Article  Google Scholar 

  32. 32.

    Wong CH, Wong SF, Pang WS, Azizah MY, Dass MJ. Habitual walking and its correlation to better physical function: implications for prevention of physical disability in older persons. J Gerontol A Biol Sci Med Sci. 2003;58(6):555–60.

    Article  PubMed  Google Scholar 

  33. 33.

    Shephard RJ. Exercise and aging: extending independence in older adults. Geriatrics. 1993;48(5):61–4.

    CAS  PubMed  Google Scholar 

  34. 34.

    Huang YJ, Chen MT, Fang CL, Lee WC, Yang SC, Kuo CHA. A possible link between exercise-training adaptation and dehydroepiandrosterone sulfate- an oldest-old female study. Int J Med Sci. 2006;3(4):141–7.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Leventhal H, Cameron L. Behavioral theories and the problem of compliance. Patient Educ Couns. 1987;10:117–38.

    Article  Google Scholar 

  36. 36.

    Sluijs EM, Kuijper EB. [Problems patients encounter in educating patients] [in Dutch]. Nederlands Tijdschrift voor Fysiotherapie. 1990;100:128–32.

    Google Scholar 

  37. 37.

    Button KS, Ioannidis JPA, Mokrysz C, Nosek BA, Flint J, Robinson ESJ, et al. Power failure: why small sample size undermines the reliability of neuroscience. Nat Rev Neurosci. 2013;14:365–76.

    CAS  Article  PubMed  Google Scholar 

  38. 38.

    Teixeira PJ, Carraça EV, Markland D, Silva MN, Ryan RM. Exercise, physical activity, and self-determination theory: a systematic review. Int J Behav Nutr Phys Act. 2012;9:78.

    Article  PubMed  PubMed Central  Google Scholar 

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The trial was funded by the Dar El Salam General Hospital (Cairo, Egypt) (reference number 1/2007), that provided facilities and equipment. The salaries of the research staff were funded by the University of Córdoba (Spain), which also provided some equipment. The research was conducted independently from the funding body.

Availability of data and materials

The raw data is available by email request to José Luis Lancho (Corresponding Author). E-mail:

Authors’ contributions

AAFB, NTF, MAG, and JLL devised the study; all authors planned and approved the experimental design and intervention; AAFB, JMR, and VMN conducted the experimental intervention; CL and MSP performed the statistical analysis; all authors drafted the paper and approved its final form. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

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Corresponding author

Correspondence to José L. Lancho.

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Bichay, A.A., Ramírez, J.M., Núñez, V.M. et al. Efficacy of treadmill exercises on arterial blood oxygenation, oxygen consumption and walking distance in healthy elderly people: a controlled trial. BMC Geriatr 16, 110 (2016).

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  • Elderly
  • Aerobic exercise
  • Cardiovascular system