Skip to content

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

A Feasibility Study of an Intervention Using a Mobile Application to Promote Strength and Balance and Reduce Risk of Falls in Older People

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02916849
Enrollment
69
Registered
2016-09-28
Start date
2016-09-30
Completion date
2017-03-31
Last updated
2017-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Accidental Falls

Keywords

Accidental Falls, Prevention & Control, Exercise, Exercise therapy/methods*, Aged, Aged 80 and over, Smartphone, Computers, Computers handheld, Motivation, Postural balance, Health behaviour, mHealth, eHealth

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.

Interventions

OTHERSafe Step

Strength and balance exercise-digital version

OTHEROEP

Strength and balance exercise -paper version

Sponsors

The Swedish Research Council
CollaboratorOTHER_GOV
Forte
CollaboratorINDUSTRY
Glasgow Caledonian University
CollaboratorOTHER
Umeå University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Adherenceafter 4 monthadherence to the program from baseline to four months

Secondary

MeasureTime frameDescription
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: Iconographical Falls Efficacy Scale (Icon-FES)baseline and four monthParticipants' falls-efficacy in certain situations
Change: Activity Specific Balance Confidence Scale (ABC)baseline and four monthParticipants' falls-efficacy in certain situations
Change: Short Physical Performance Batterybaseline and four monthStanding balance, leg muscle strength in chair stand, and gait speed
Change: 30 second chair-standbaseline and four monthLeg muscle strength in chair stand
Usability of the programsUp to four monthsInterviews and observations
UptakebaselineProportion of invited participants that accepted and started the program.
Change: Late-Life Function and Disability Instrument (LLFDI)baseline and four montha person's ability to do discrete actions or activities, and disability-a person's performance of socially defined life tasks

Other

MeasureTime frameDescription
Background dataBaselineBefore the study the participants will fill in a questionnaire with background data containing: self-reported health, medical diagnoses, medication, age, sex, earlier work, computer skill and number of falls previous year.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026