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Table 2 A brief structured summary of the RCT part of the promoting aging migrants’ capabilities study *

From: A person-centred approach to health promotion for persons 70+ who have migrated to Sweden: promoting aging migrants’ capabilities implementation and RCT study protocol

Data category

Information

Primary registry and trial identifying number

ClinicalTrials.gov NCT01841853

Date of registration in primary registry

10 April 2013

Secondary identifying numbers

-

Source(s) of monetary or material support

The Swedish Research Council, the Centre for Person-Centred Care (GPCC) at Gothenburg University, Sweden

Primary sponsor

The University of Gothenburg, Sweden

Secondary sponsor(s)

The City of Gothenburg, Sweden

The Region of Västra Götaland, Sweden

Contact for public queries

SDI, synneve.dahlin-ivanoff@.gu.se

Contact for scientific queries

SDI, synneve.dahlin-ivanoff@.gu.se, the Sahlgrenska Academy at the University of Gothenburg, Institute of Neuroscience and Physiology/Section for Health and Rehabilitation, Sweden

Public title

The Promoting Aging Migrants’ Capabilities Study

Scientific title

The Promoting Aging Migrants’ Capabilities Study: a person-centred approach to health promotion for persons 70+ who have migrated to Sweden

Countries of recruitment

Sweden

Health condition(s) or problem(s) studied

Health promotion for older persons born abroad

Intervention(s)

Intervention: 4 senior meetings and 1 follow-up home visit

Control: Conventional care and follow-up

Key inclusion and exclusion criteria

Ages eligible for study: ≥ 70 years; Sexes eligible for study: both; Accepts healthy volunteers: Yes

Inclusion criteria: adult person (≥70 years); born in Finland or any of the four countries in the Balkan Peninsula; living in an urban district in a medium-sized city; living in ordinary housing; not dependent on informal or formal help in daily activities

Exclusion criteria: impaired cognition [Mini Mental State Examination (MMSE) below 80% of administered items]

Study type

Interventional

Allocation: randomised; Intervention model: parallel assignment; Masking: non-blind

Primary purpose: Health promotion

Phase III

Date of first enrolment

08 August 2012

Target sample size

130

Recruitment status

Recruiting

Primary outcome

Activities of Daily Living (ADL)

Key secondary outcomes

Frailty indicators, falls and fear of falls, symptoms, depression, healthcare consumption, self-rated health, life satisfaction, leisure activities, assistive technology, and social support

  1. *WHO Trial Registration Data Set.