Prospective RELOC-AGE: How Do Housing Choices and Relocation Matter for Active Ageing? (RELOC-AGE)

October 3, 2023 updated by: Susanne Iwarsson, Lund University
The objective of prospective RELOC-AGE is to study housing choices and relocation and to examine the effects on active ageing among people aged 55+ considering relocation. All data collection will be conducted at baseline and after 1, 3, 5 and 7 years of follow-up.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

The objective of prospective RELOC-AGE is to study housing choices and relocation and to examine the effects on active ageing among people aged 55+ considering relocation.

Research Questions

  1. What aspects of housing, health and participation predict a) relocation to different housing options in the ordinary housing stock; b) residential care facilities; c) remaining in the present dwelling?
  2. How is the complex interaction between objective and perceived aspects of housing, health and participation associated with active ageing, and what are the patterns and characteristics of such dynamics?
  3. What housing attributes do people aged 55+ considering relocation find important, and to what extent, when making their decisions on housing preferences?
  4. How do people aged 55+ considering relocation reason a) regarding different housing options; b) motives for considering and effectuating relocation, and; c) to what extent are their motives fulfilled?

The sample will include people aged 55+ considering relocation. Recruitment will be made from a sub-sample based on waiting lists (n=22 000) among three housing companies in Sweden: Karlshamnsbostäder AB, Örebrobostäder AB, and Riksbyggen. The expected final sample size is n=3000. Quantitative data will be collected through a web survey and one telephone interview at baseline (2021) and by a web survey at follow-ups 2022, 2024, 2026 and 2028. Data on primary and secondary outcomes are based on established questionnaires used in previous research on older people, health, and housing as well as in national public health surveys in Sweden. In addition to primary and secondary outcomes (presented below), the surveys include demographic and socioeconomic characteristics including civil status, education level, economic situation, occupational status, holding a driver license, critical life events (e.g., death of spouse, long-term disease, divorce), original nationality; questions about present housing situation (dwelling characteristics (e.g., type and size of dwelling, location) and neighborhood characteristics (e.g., access to services and green areas), potential and realized mobility, social/cohabiting situation, time spent at home, housing adaptations); use of technical aids for mobility, use of health, social and informal care, thoughts about future housing, reasons related to consideration about relocating and moving intentions. Data on stated preferences in relation to housing will be collected in a specific survey based on a discrete choice methodology. Qualitative interviews will be conducted consecutively with a subsample (n=100) of respondents who have relocated during the follow-up period. Further, linking to register data will be made within the scope of Register RELOC-AGE, which is another part of the larger project.

For quantitative data, descriptive, exploratory, and inferential statistics will be used. For longitudinal analyses, generalized linear models or Cox regression with time-dependent covariates will be applied. Throughout, we will control for demographic and socioeconomic characteristics and other potential confounders and compare the results across different cohorts. Quantitative analyses will be conducted using standard statistical software. For analyses of DCE data, we will use the conditional logit model (also referred to as the multinomial logit model) as the reference model, but the analysis will be extended to mixed logit and latent class models to take preference heterogeneity into account. Qualitative interviews will be audio-recorded and transc¬ribed verbatim and principles from Grounded Theory will be used for the analysis.

Study Type

Observational

Enrollment (Actual)

1964

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Lund, Sweden, 22120
        • Active and Healthy Ageing Research Group, Department of Health Sciences Lund University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

55 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Persons 55 years or older, living in Sweden, listed for relocation at any of the three housing companies Karlshamnsbostäder and Örebrobostäder (public housing companies) and Riksbyggen (a condominium provider)

Description

Inclusion Criteria:

  • Persons 55 years or older, living in Sweden, listed for relocation at any of the three housing companies Karlshamnsbostäder and Örebrobostäder (public housing companies) and Riksbyggen (a condominium provider)

Exclusion Criteria:

  • Severe cognitive impairments or insufficient language skills to give informed consent and participate in telephone interviews

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Persons 55 years or older considering relocation
No intervention is administered.
No intervention is administered, the cohort is followed in order to evaluate the impact of housing and relocation on active ageing outcomes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
University of Jyväskylä Active Aging Scale (UJACAS)
Time Frame: Change from Baseline Active Ageing score to 12 months
17 items(areas of activity), each to be self-rated regarding goals, ability, autonomy and activity (total scores 0-272)
Change from Baseline Active Ageing score to 12 months
University of Jyväskylä Active Aging Scale (UJACAS)
Time Frame: Change from Baseline Active Ageing score to 24 months
17 items(areas of activity), each to be self-rated regarding goals, ability, autonomy and activity (total scores 0-272)
Change from Baseline Active Ageing score to 24 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Life-space mobility
Time Frame: Change from Baseline Life-space mobility to 12 months
6 items related to life spaces visited during the past four weeks, whether the person had visited (yes/no), frequency on a four-point scale, and level of dependence on others or technical equipment on a three-point scale)
Change from Baseline Life-space mobility to 12 months
Life-space mobility
Time Frame: Change from Baseline Life-space mobility to 24 months
6 items related to life spaces visited during the past four weeks, whether the person had visited (yes/no), frequency on a four-point scale, and level of dependence on others or technical equipment on a three-point scale)
Change from Baseline Life-space mobility to 24 months
Meaning of home
Time Frame: Change from Baseline Meaning of home scores to 12 months
28 items with statements to which respondents state agreement on a ten-point scale from 1 (not at all) to 10 (very much)
Change from Baseline Meaning of home scores to 12 months
Meaning of home
Time Frame: Change from Baseline Meaning of home scores to 24 months
28 items with statements to which respondents state agreement on a ten-point scale from 1 (not at all) to 10 (very much)
Change from Baseline Meaning of home scores to 24 months
Housing related control beliefs
Time Frame: Change from Baseline Housing related control beliefs scores to 12 months
24 items with statements to which respondents state agreement on a five-point scale from 1 (not at all) to 5 (very much)
Change from Baseline Housing related control beliefs scores to 12 months
Housing related control beliefs
Time Frame: Change from Baseline Housing related control beliefs scores to 24 months
24 items with statements to which respondents state agreement on a five-point scale from 1 (not at all) to 5 (very much)
Change from Baseline Housing related control beliefs scores to 24 months
Usability in my home
Time Frame: Change from Baseline Usability in my home scores to 12 months
4 items (selected from original instrument) with statements about aspects of usability rated on a five-point scale from 1 (not at all) to 5 (very much)
Change from Baseline Usability in my home scores to 12 months
Usability in my home
Time Frame: Change from Baseline Usability in my home scores to 24 months
4 items (selected from original instrument) with statements about aspects of usability rated on a five-point scale from 1 (not at all) to 5 (very much)
Change from Baseline Usability in my home scores to 24 months
Housing satisfaction
Time Frame: Change from Baseline Housing satisfaction scores to 12 months
One item "Are you happy with the condition of your home?" answered on a five-point scale from 1 (definitely not) to 5 ('yes, definitely)
Change from Baseline Housing satisfaction scores to 12 months
Housing satisfaction
Time Frame: Change from Baseline Housing satisfaction scores to 24 months
One item "Are you happy with the condition of your home?" answered on a five-point scale from 1 (definitely not) to 5 ('yes, definitely)
Change from Baseline Housing satisfaction scores to 24 months
Health-related Quality of life
Time Frame: Change from Baseline Health-related Quality of Life to 12 months
EuroQol-5d questionnaire (5 items, range 1-5 per item, with higher score indicating worse outcome)
Change from Baseline Health-related Quality of Life to 12 months
Health-related Quality of life
Time Frame: Change from Baseline Health-related Quality of Life to 24 months
EuroQol-5d questionnaire (5 items, range 1-5 per item, with higher score indicating worse outcome)
Change from Baseline Health-related Quality of Life to 24 months
Self-rated health
Time Frame: Change from Baseline Self-rated Health to 12 months
One item "How would you rate your own health", rated from 1 (bad) to 5 (excellent)
Change from Baseline Self-rated Health to 12 months
Self-rated health
Time Frame: Change from Baseline Self-rated Health to 24 months
One item "How would you rate your own health", rated from 1 (bad) to 5 (excellent)
Change from Baseline Self-rated Health to 24 months
Life satisfaction
Time Frame: Change from Baseline Life satisfaction to 12 months
One item "How satisfied are you with life in general", rated from 1 (very unsatisfied) to 6 (very satisfied)
Change from Baseline Life satisfaction to 12 months
Life satisfaction
Time Frame: Change from Baseline Life satisfaction to 24 months
One item "How satisfied are you with life in general", rated from 1 (very unsatisfied) to 6 (very satisfied)
Change from Baseline Life satisfaction to 24 months
Housing enabler, functional limitations
Time Frame: Change from Baseline Functional limitations to 12 months
8 items indicating presence (yes or yes to some extent) /absence (no) functional limitations
Change from Baseline Functional limitations to 12 months
Housing enabler, functional limitations
Time Frame: Change from Baseline Functional limitations to 24 months
8 items indicating presence (yes or yes to some extent) /absence (no) functional limitations
Change from Baseline Functional limitations to 24 months
General self-efficacy
Time Frame: Change from Baseline Genreal Self-efficacy to 12 months
10 items with statements to which respondents state agreement on a four-point scale from 1 (completely disagree) to 4 (totally agree)
Change from Baseline Genreal Self-efficacy to 12 months
General self-efficacy
Time Frame: Change from Baseline Genreal Self-efficacy to 24 months
10 items with statements to which respondents state agreement on a four-point scale from 1 (completely disagree) to 4 (totally agree)
Change from Baseline Genreal Self-efficacy to 24 months
Physical exercise
Time Frame: Change from Baseline physical exercise duration/week to 12 months
Rated as duration per week on five levels from 0 minutes to 2 hours or more
Change from Baseline physical exercise duration/week to 12 months
Physical exercise
Time Frame: Change from Baseline physical exercise duration/week to 24 months
Rated as duration per week on five levels from 0 minutes to 2 hours or more
Change from Baseline physical exercise duration/week to 24 months
Physical activity
Time Frame: Change from Baseline physical activity duration/week to 12 months
Rated as duration per week on six levels from 0 minutes to 2 hours or more
Change from Baseline physical activity duration/week to 12 months
Physical activity
Time Frame: Change from Baseline physical activity duration/week to 24 months
Rated as duration per week on six levels from 0 minutes to 2 hours or more
Change from Baseline physical activity duration/week to 24 months
Frailty (FRESCH)
Time Frame: Change from Baseline Frailty scores to 12 months
4 items to be answered yes or no
Change from Baseline Frailty scores to 12 months
Frailty (FRESCH)
Time Frame: Change from Baseline Frailty scores to 24 months
4 items to be answered yes or no
Change from Baseline Frailty scores to 24 months
Satisfaction with mobility opportunities
Time Frame: Change from Baseline Satisfaction with mobility opportunities to 12 months
One item, rated from 1 (very satisfied) to 5 (very unsatisfied)
Change from Baseline Satisfaction with mobility opportunities to 12 months
Satisfaction with mobility opportunities
Time Frame: Change from Baseline Satisfaction with mobility opportunities to 24 months
One item, rated from 1 (very satisfied) to 5 (very unsatisfied)
Change from Baseline Satisfaction with mobility opportunities to 24 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2021

Primary Completion (Estimated)

December 31, 2028

Study Completion (Estimated)

June 30, 2029

Study Registration Dates

First Submitted

February 16, 2021

First Submitted That Met QC Criteria

February 19, 2021

First Posted (Actual)

February 21, 2021

Study Record Updates

Last Update Posted (Actual)

October 5, 2023

Last Update Submitted That Met QC Criteria

October 3, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2020-03457

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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