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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03059199
Other study ID # H1600736
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 20, 2016
Est. completion date June 22, 2018

Study information

Verified date October 2018
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research is to implement and evaluate the feasibility of the HAT- TRICK Program, a gender- sensitive intervention program targeting physical activity, healthy eating and connectedness in men living in the Okanagan Region, BC.


Description:

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Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Single-Arm Feasibility Study
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.

Locations

Country Name City State
Canada Prospera Place Kelowna British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Canadian Cancer Society Research Institute (CCSRI)

Country where clinical trial is conducted

Canada, 

References & Publications (2)

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. — View Citation

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 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Program Feasibility 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 Dietary Behaviour Measured by the Dietary Instrument for Nutrition Education (DINE) questionnaire. Baseline, Post-Intervention (12-weeks), and 9-month follow-up
Secondary Physical Activity Behaviour 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
Secondary Anthropometrics Measures of height, weight, waist circumference, and blood pressure Baseline, Post-Intervention (12-weeks), and 9-month follow-up
Secondary Health-Related Quality of Life 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
Secondary Social Connectedness Measured using the Abbreviated Duke Social Support Scale. Baseline, Post-Intervention (12-weeks), and 9-month follow-up
Secondary Alcohol Consumption Measured using a 7-day alcohol recall. Baseline, Post-Intervention (12-weeks), and 9-month follow-up
Secondary Sedentary Behaviour Measured using the Marshall Sitting Questionnaire. Baseline, Post-Intervention (12-weeks), and 9-month follow-up
Secondary Risk of Depression Measured using the Male Depression Risk Scale. Baseline, Post-Intervention (12-weeks), and 9-month follow-up
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