- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04765696
Prospective RELOC-AGE: How Do Housing Choices and Relocation Matter for Active Ageing? (RELOC-AGE)
Study Overview
Status
Conditions
Intervention / Treatment
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
- 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?
- 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?
- What housing attributes do people aged 55+ considering relocation find important, and to what extent, when making their decisions on housing preferences?
- 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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Lund, Sweden, 22120
- Active and Healthy Ageing Research Group, Department of Health Sciences Lund University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
Sponsor
Collaborators
Investigators
- Study Chair: Agneta Malmgren Fänge, PhD, Lunds University
Publications and helpful links
General Publications
- Zingmark M, Nordestrom F, Iwarsson S. Challenges related to self-assessment of active ageing during the Covid-19 pandemic in Sweden. BMC Res Notes. 2022 May 13;15(1):171. doi: 10.1186/s13104-022-06059-3.
- Zingmark M, Bjork J, Granbom M, Gefenaite G, Nordestrom F, Schmidt SM, Rantanen T, Slaug B, Iwarsson S. Exploring Associations of Housing, Relocation, and Active and Healthy Aging in Sweden: Protocol for a Prospective Longitudinal Mixed Methods Study. JMIR Res Protoc. 2021 Sep 21;10(9):e31137. doi: 10.2196/31137.
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Active Ageing
-
Centre Hospitalier Universitaire de NiceRecruiting
-
Lund UniversityThe Swedish Research Council; Linnaeus UniversityCompleted
-
Norwegian University of Science and TechnologyCompleted
-
University of GlasgowCompleted
-
University of SouthamptonNational Institute for Health Research, United KingdomUnknown
-
Assistance Publique - Hôpitaux de ParisUnknown
-
Wageningen UniversityCompleted
-
Quadram Institute BioscienceNorfolk and Norwich University Hospitals NHS Foundation TrustActive, not recruitingAgeingUnited Kingdom
-
University Hospital, LimogesCompleted
-
Wageningen UniversityRecruiting
Clinical Trials on No intervention is administered
-
National Opinion Research CenterChapin Hall at the University of Chicago; Office of Planning, Research & Evaluation and other collaboratorsRecruiting
-
University of SouthamptonUniversity Hospital Southampton NHS Foundation Trust; National Institute for... and other collaboratorsRecruitingHuntington DiseaseUnited Kingdom
-
Oregon Health and Science UniversityMassachusetts General Hospital; National Eye Institute (NEI); University of Illinois... and other collaboratorsRecruiting
-
Exactis InnovationKnight TherapeuticsCompleted
-
University of Dublin, Trinity CollegeCompleted
-
Biosplice Therapeutics, Inc.Completed
-
NHS GrampianCompleted
-
Pirogov Russian National Research Medical UniversityCompletedChronic Venous InsufficiencyRussian Federation
-
Eisai Inc.CompletedEpilepsy | Primary Generalized Tonic-Clonic Seizures | Partial-Onset Seizures