MedPath

A Feasibility Study of a Mobile Application Intervention to Promote Strength and Balance Exercises in Older People

Not Applicable
Completed
Conditions
Accidental Falls
Registration Number
NCT02916849
Lead Sponsor
Umeå University
Brief Summary

This five arm feasibility study aims to promote self-management in strength and balance exercises among community-living older people. The research process, implementation strategies and procedures, acceptability of the exercise programs, perceived benefits of the programs, and the ecological validity, acceptability and ability to detect change of possible outcome measurements will be evaluated before a future randomized controlled trial. A comparison of two exercise programs will be performed; a) Safe Step, a mobile technology based exercise program with motivational strategies, developed by researchers in collaboration with older adults, and b) Otago Exercise Program (OEP), home exercises presented in a booklet. The older participants will be free to select either of the intervention programs and the selection process and outcome will be studied as part of the process evaluation.

The participants in three of the arms (OEP, Safe Step, and Safe Step with mentors) will be recruited through advertisements in local papers and through posters and meetings at senior citizens organisations. In the fourth and fifth arms (OEP and Safe Step) the participants will be recruited from health care centres and their registered professionals with experience of greens prescriptions (Fysisk aktivitet på recept). All five groups, with at least 10 participants in each, will be exercising for four months and will undergo testing at baseline, after two and four months and they will be asked to keep an exercise diary (digital or paper format) during the intervention.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
69
Inclusion Criteria
  • Independently living
  • Able to rise from a high chair
  • Able to stand without support
  • Experience an impaired balance
Exclusion Criteria
  • Progressive disease that impairs mobility
  • Dementia diagnosis
  • Intense exercising more than 3 hours / week

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Adherenceafter 4 month

adherence to the program from baseline to four months

Secondary Outcome Measures
NameTimeMethod
Change: Late-Life Function and Disability Instrument (LLFDI)baseline and four month

a person's ability to do discrete actions or activities, and disability-a person's performance of socially defined life tasks

Change: Attitudes to Falls-Related Interventions Scale (AFRIS)baseline, two month and four month
Change: Behavioural Regulation In Exercise Questionnaire (BREQ-2)baseline, two month and four month
Change: 30 second chair-standbaseline and four month

Leg muscle strength in chair stand

Usability of the programsUp to four months

Interviews and observations

Change: Iconographical Falls Efficacy Scale (Icon-FES)baseline and four month

Participants' falls-efficacy in certain situations

Change: Activity Specific Balance Confidence Scale (ABC)baseline and four month

Participants' falls-efficacy in certain situations

Change: Short Physical Performance Batterybaseline and four month

Standing balance, leg muscle strength in chair stand, and gait speed

Uptakebaseline

Proportion of invited participants that accepted and started the program.

Trial Locations

Locations (1)

Caring Science Buildning, Umeå University

🇸🇪

Umeå, Sweden

Caring Science Buildning, Umeå University
🇸🇪Umeå, Sweden

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.