HAT TRICK: An Innovative Health Promotion Program for Men
HAT TRICK: Examining the Feasibility of a Gender Sensitive Intervention Focused on Physical Activity, Healthy Eating and Connectedness in Male Hockey Fans
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
British Columbia
-
Kelowna, British Columbia, Canada
- Prospera Place
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Men over the age of 35 years
- Residing in the Okanagan Region of British Columbia Canada
- Accumulate <150mins of moderate to vigorous physical activity a week
- Have a BMI >25kg/m2
- Pant size of >38"
Exclusion Criteria:
- No specific exclusion criteria
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Single-Arm Feasibility Study
12-week, 1x/week, 90-minute face-to-face sessions.
|
Participants are provided with the HAT TRICK Playbook, a resource manual including weekly healthy eating and physical activity challenges and tracking logs.
Each face-to-face session is facilitated by trained research staff, community partners, and health care professionals.
Weekly sessions include information on physical activity, healthy eating, and behaviour change techniques (e.g., social support, goal setting, self-monitoring) and include an opportunity to be active/exercise.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Program Feasibility
Time Frame: Post-Intervention (12-weeks)
|
Program feasibility will be evaluated using mixed-methods to explore program delivery, recruitment, participant and facilitator satisfaction, challenges and issues faced during the program, and recommended changes to the program.
Methods for collecting feasibility data will include: 1) program satisfaction/acceptability questionnaire for all participants; 2) semi-structured telephone interviews with a sub-sample of the HAT TRICK participant (telephone interviews provide rich qualitative data and are time & resource efficient; 3) semi-structured interviews with guest presenters and club 'insiders'.
|
Post-Intervention (12-weeks)
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dietary Behaviour
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured by the Dietary Instrument for Nutrition Education (DINE) questionnaire.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Physical Activity Behaviour
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured using the Actigraph GT3X+© accelerometer and Godin's Leisure Time Exercise Questionnaire (GLTEQ).
The Actigraph GT3X+©, which is the 'gold standard' measure of physical activity in adults, will be worn by all participants during all waking hours over 7 consecutive days.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Anthropometrics
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measures of height, weight, waist circumference, and blood pressure
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Health-Related Quality of Life
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Health-related quality of life will be assessed using the validated SF-12V2 Health Survey.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Social Connectedness
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured using the Abbreviated Duke Social Support Scale.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Alcohol Consumption
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured using a 7-day alcohol recall.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Sedentary Behaviour
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured using the Marshall Sitting Questionnaire.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
|
Risk of Depression
Time Frame: Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Measured using the Male Depression Risk Scale.
|
Baseline, Post-Intervention (12-weeks), and 9-month follow-up
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Cristina Caperchione, PhD, UBCO Health and Exercise Sciences
Publications and helpful links
General Publications
- Caperchione CM, Bottorff JL, Oliffe JL, Johnson ST, Hunt K, Sharp P, Fitzpatrick KM, Price R, Goldenberg SL. The HAT TRICK programme for improving physical activity, healthy eating and connectedness among overweight, inactive men: study protocol of a pragmatic feasibility trial. BMJ Open. 2017 Sep 6;7(9):e016940. doi: 10.1136/bmjopen-2017-016940.
- Sharp P, Bottorff JL, Hunt K, Oliffe JL, Johnson ST, Dudley L, Caperchione CM. Men's Perspectives of a Gender-Sensitized Health Promotion Program Targeting Healthy Eating, Active Living, and Social Connectedness. Am J Mens Health. 2018 Nov;12(6):2157-2166. doi: 10.1177/1557988318799159. Epub 2018 Sep 20.
- Sharp P, Bottorff JL, Oliffe JL, Hunt K, Caperchione CM. Process evaluation of HAT TRICK: feasibility, acceptability and opportunities for programme refinement. Health Educ Res. 2020 Dec 23;35(6):605-617. doi: 10.1093/her/cyaa029.
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
Other Study ID Numbers
- H1600736
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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.
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