"I am a Physically Active Person!": A Randomized Controlled Trial Aimed to Increase Levels of Physical Activity Self-Definition and Physical Activity Among a Sample of Inactive Adults
1 other identifier
interventional
120
0 countries
N/A
Brief Summary
This explanatory sequential mixed methods study investigated if an intervention can increase the physical activity identity and physical activity (PA) of inactive individuals. The intervention condition focused on increasing participant's physical activity self-definition (PASD) through educational sessions and group discussions on the five direct and indirect determinants of PASD (perceived enjoyment, perceived wanting, perceived commitment, perceived trying, perceived ability). The control condition was given general health behaviour education sessions. Researchers conducted interviews with some of the participants after the intervention was completed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2015
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2017
CompletedFirst Submitted
Initial submission to the registry
June 28, 2024
CompletedFirst Posted
Study publicly available on registry
July 19, 2024
CompletedJuly 22, 2024
June 1, 2024
1.6 years
June 28, 2024
July 18, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Physical Activity Self-Definition
Measured with a 4-item questionnaire using a 7-point Likert scale (1= strongly disagree; 7 = strongly agree)
Measured pre-intervention, 5 weeks later at intervention end and 4 weeks post intervention
ActiGraph Accelerometers
Weekly sedentary, light, moderate, and vigorous physical activity minutes were measured using accelerometers, worn at the hip for 7 day during waking hours.
Measured pre-intervention, 5 weeks later at intervention end and 4 weeks post intervention
Study Arms (2)
PASD Intervention
EXPERIMENTAL6 week 30-45 minute psychoeducation sessions that delivered content on the variables within the Physical Activity Self-Definition Model. The first session was an introductory session and each one that followed focused on one of the direct or indirect determinants of the model: perceived enjoyment, perceived wanting, perceived commitment, perceived trying, perceived ability (all relating to physical activity). Group activities such as worksheets and discussion were carried out during the session.
Attention Control
ACTIVE COMPARATOR6 week 30-45 minute educational sessions that delivered content on general health behaviour. After the introductory session, each week, one of five general health behaviours were covered: balanced diet, sleep, reducing sedentary behaviour, mental/spiritual health and self-compassion/cultivating positive health behaviours. Group activities such as worksheets and discussion were carried out during the session.
Interventions
6 week behavioural change program designed to increase PASD and PA
6 week program designed to as an attention control, delivering content on general health behaviour.
Eligibility Criteria
You may qualify if:
- Must be insufficiently active (\<150 minutes of moderate-vigorous PA per week)
- Scored below the mean in PASD
- Medically safe to participate in PA
- Intention to engage in PA over the next 6 weeks
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Manitobalead
- Research Manitobacollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- The participants were told that they were in one of two informational sessions; they were not told if they were in the intervention or the control group. Researchers sending the surveys to participants' emails were also blinded to the condition. Intervention facilitators who were presenting the material were necessarily aware of the condition.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 28, 2024
First Posted
July 19, 2024
Study Start
September 1, 2015
Primary Completion
April 1, 2017
Study Completion
April 1, 2017
Last Updated
July 22, 2024
Record last verified: 2024-06
Data Sharing
- IPD Sharing
- Will not share
We do not have ethics approval to share data