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SMS Reminders for Exercise Among Older Adults. Malaysian Physical Activity for Health Study

Promoting Exercise Among Older Malaysians Using SMS Reminders. The Malaysian Physical Activity for Health Study (myPAtHS): A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02123342
Acronym
myPAtHS
Enrollment
43
Registered
2014-04-25
Start date
2014-06-30
Completion date
2015-01-31
Last updated
2015-05-27

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

Conditions

Exercise, Physical Activity

Keywords

health, older adults, mobile phone

Brief summary

The purpose of the study is: 1\) To evaluate the efficacy and feasibility of an SMS reminder intervention for promoting an health-related exercise programme (myPAtHS) among older Malaysian adults, in a randomized controlled trial (RCT). Hypothesis: Frequency and duration of the exercise programme execution will be higher for the SMS reminder condition compared to the programme only condition. The effect may be reduced from post- to follow-up measurement (24 weeks after baseline and 12 weeks after post-measurement) but all outcomes will remain significantly higher at 24 weeks.

Interventions

BEHAVIORALExercise programme plus SMS reminders

Participants will receive SMS reminders for their myPAtHS exercise programme compared to the other group where participants will only receive the myPAtHS exercise programme.

Sponsors

University of Malaya
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
55 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Mobile phone user * Acceptable health that does not prevent exercise * Acceptable command of the English language * No engagement in a regular- structured exercise routine like gym training or other structured programmes * Interest in an exercise programme * Willing to attend scheduled follow-up sessions at 12 weeks (pre-post evaluation) and 24 weeks (post-intervention evaluation) after the first session

Exclusion criteria

* participants who have any medical condition or health concern that would restrict regular exercise based on one screening question. If this question will be answered with yes participants are advised to seek medical care.

Design outcomes

Primary

MeasureTime frameDescription
Number of myPAtHS exercise sessions.12 weeks & 24 weeksThis will be assessed with an exercise diary.
Time spent doing the myPAtHS exercise programme.12 weeks & 24 weeksThis will be assessed with an exercise diary.

Secondary

MeasureTime frameDescription
Change in overall physical activity.baseline, 12 weeks & 24 weeksThe International Physical Activity Questionnaire (short version) will be used to collect physical activity data.
Change in exercise self-efficacy.baseline, 12 weeks & 24 weeksThe Exercise Self-Efficacy-Scale will be used to collect exercise self-efficacy data.
Change in grip strength.baseline, 12 weeks & 24 weeksGrip strength will be assessed using the North Coast strength dynamometer (North Coast Hydraulic Hand Dynamometer, North Coast Medical Inc, Morgan Hill, California, USA).
Change in leg-strength.baseline, 12 weeks & 24 weeksLeg-strength will be collected using the 30 seconds chair-stand-test.
Subjective intensity while doing the myPAtHS exercise programme.12 weeks & 24 weeksThis will be assessed with an exercise diary.

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026