CClinicalTrials.gg
CompletedNCT03636282Updated Jun 7, 2023

Hockey Fans in Training (Hockey FIT): Improving Men's Health Through the Power of Sport

An interventional study of Hockey FIT Program (Immediate Delivery) in Overweight and Obesity, sponsored by Western University, Canada. Completed at 40 sites in 2 countries. Open to male participants aged 35 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-06-07.

Sponsored by Western University, Canada · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
997
Allocation
Randomized
Ages
35 Years to 65 Years
Sex
Male
01

Study summary

Hockey Fans in Training (Hockey FIT) is a 12-month (3-month active phase and 9-month minimally-supported phase) weight loss and healthy lifestyle program for middle-aged, male hockey fans with overweight or obesity, delivered by trained coaches in collaboration with major junior or professional hockey teams and implementation partners (e.g., YMCAs, local fitness facilities, and universities) in Canada and the United States.

In the proposed study, a minimum of 32 sites (affiliated with hockey teams and local implementation partners) will be randomly assigned to either immediate delivery (Hockey FIT program) or delayed delivery (wait-list control). At each site, male hockey fans at risk for chronic diseases will be recruited to take part in the study (note: the goal is to recruit approximately 40 men/site). Sites assigned to the delayed delivery group will offer the Hockey FIT program to their enrolled participants after 12 months.

Through the Hockey FIT program, the investigators aim to promote weight loss, increase physical activity levels, and improve other health measures through a cost-effective solution that is acceptable and appealing to men who have overweight or obesity.

Read the detailed description

The overall goal of this study is to reduce preventable chronic diseases in men by improving health behaviours and health indicators. To achieve this goal, following a successful pilot study providing strong evidence to proceed with a definitive trial, the investigators are conducting a pragmatic, cluster randomized controlled trial (RCT) of the Hockey FIT program.

The primary specific aim is to conduct an outcome evaluation to evaluate the effectiveness of Hockey FIT in middle-aged men who have overweight or obesity. Specifically, the investigators will: examine whether Hockey FIT (vs. wait-list control) leads to: greater weight loss at 12 months (primary outcome), as well as improved health behaviours (physical activity; sedentary time; eating habits) and health indicators (physiological measures; health \& psychosocial measures) at 3 and 12 months.

Following the pilot study, the investigators will use the affiliation of being a fan of hockey as a powerful draw to engage men. Sites will be selected based on availability of both a major junior (or professional) hockey team and an implementation partner (e.g., YMCA branch, fitness facility, University) located in the city. A minimum of 32 sites in Canada and the United States will be randomized to the intervention (Hockey FIT program: immediately delivery) or comparator (wait-list control: delayed delivery); at each site, men will be recruited to participate (with the goal of recruiting approximately 40 men/site). Intervention sites will begin Hockey FIT immediately while comparator sites will offer Hockey FIT after a 12-month delay. The measurement sessions involving both groups will take place at 0 (baseline), 3 and 12 months.

02

Conditions studied

  • Overweight
  • Obesity

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Keywords

  • Chronic disease
  • Men's health
  • Health promotion
  • Exercise
  • Healthy diet
  • Health Technology
  • Weight loss
  • Hockey
03

In context

Overweight

3,670 studies on the registry are indexed under Overweight; 849 are open to participants now.

This study's enrollment of 997 is above the median of 73 across 3,175 interventional studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

Western University, Canada is the lead sponsor of 221 studies on the registry; 56 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
35 Years to 65 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Male;
  2. Between 35 and 65 years of age;
  3. Objectively-measured body-mass index of at least 27 kg/m2
  4. Deemed safe to participate in physical activity [i.e., clear the 2018 Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) or receive written clearance from a health care provider].

Exclusion criteria

Exclusion Criteria:

  1. Advised by a health care provider to not participate in the program
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
997 participants (actual)

Study arms

  • Experimental
    Hockey FIT Program (Immediate Delivery)

    Hockey FIT Program: A gender-sensitized, weight loss and healthy lifestyle program that engages men using the power of being a sports fan.

    Behavioral: Hockey FIT Program (Immediate Delivery)

  • No intervention
    Wait-List Control (Delayed Delivery)

    No intervention for 12 months. After 12 months, Hockey FIT program is offered.

Interventions

  • BehavioralHockey FIT Program (Immediate Delivery)

    Hockey FIT is comprised of a 3-Month Active Phase and a 9-Month Minimally-Supported Phase. Active Phase: 12 weekly, 90-minute group-based sessions consisting of classroom-based education and exercise. Outside of sessions, participants follow their individualized lifestyle prescriptions for healthy eating, physical activity (steps), and exercise. Participants are encouraged to regularly use health technology support tools customized to Hockey FIT. Minimally-supported phase: Participants are encouraged to continue with their healthy lifestyle behaviour changes and to regularly use the health technology support tools.

06

What researchers measure

Primary outcomes

  1. Weight loss (absolute)

    Measured using a digital weight scale (in kg)

    Time frame: 12 months

Secondary outcomes

  1. Weight loss (absolute)

    Measured using a digital weight scale (in kg)

    Time frame: 3 months

  2. Weight loss (percent change)

    Measured using a digital weight scale (% change from baseline)

    Time frame: 3 months & 12 months

  3. Predicted maximal oxygen uptake (VO2max)

    Calculated from sub-maximal fitness test (in mL/kg/min)

    Time frame: 3 months & 12 months

  4. Systolic blood pressure

    Measured using an automated blood pressure monitor (in mm Hg)

    Time frame: 3 months & 12 months

  5. Diastolic blood pressure

    Measured using an automated blood pressure monitor (in mm Hg)

    Time frame: 3 months & 12 months

  6. Body mass index

    Calculated from weight (digital weight scale) and height (portable stadiometer) (in kg/m2)

    Time frame: 3 months & 12 months

  7. Waist circumference

    Measured using tape measure (in cm)

    Time frame: 3 months & 12 months

  8. Glycated hemoglobin (A1c)

    Measured using a point-of-care analyzer (%)

    Time frame: 3 months & 12 months

  9. Daily steps

    Measured using a waist-worn accelerometer-based step counter over 7 days (average steps/day)

    Time frame: 3 months & 12 months

  10. Total physical activity MET-minutes/week

    Measured using the International Physical Activity Questionnaire (IPAQ) - Short Form (sum of Walking + Moderate + Vigorous MET-minutes/week)

    Time frame: 3 months & 12 months

  11. Vigorous physical activity MET-minutes/week

    Measured using the International Physical Activity Questionnaire (IPAQ) - Short Form (calculated as 8.0 \* vigorous-intensity activity minutes \* vigorous-intensity days)

    Time frame: 3 months & 12 months

  12. Moderate physical activity MET-minutes/week

    Measured using the International Physical Activity Questionnaire (IPAQ) - Short Form (calculated as 4.0 \* moderate-intensity activity minutes \* moderate-intensity days)

    Time frame: 3 months & 12 months

  13. Walking MET-minutes/week

    Measured using the International Physical Activity Questionnaire (IPAQ) - Short Version (calculated as 3.3 \* walking minutes \* walking days)

    Time frame: 3 months & 12 months

  14. Total time spent sitting (on a week day)

    Measured using the Marshall Questionnaire (in minutes)

    Time frame: 3 months & 12 months

  15. Healthful eating score

    Measured using the Starting the Conversation (STC) Questionnaire (summary score of 8 items; score range, 0-16; lower score indicates more healthful eating)

    Time frame: 3 months & 12 months

  16. Fruit and vegetable intake

    Measured using the Canadian Community Health Survey

    Time frame: 3 months & 12 months

  17. Sweetened sugary beverages intake

    Measured using the Behavioral Risk Factor Surveillance System Questionnaire

    Time frame: 3 months & 12 months

  18. Total alcohol intake (weekly)

    Measured using a 7-day recall diary

    Time frame: 3 months & 12 months

  19. Smoking status

    Measured using questions adapted from the Canadian Community Health Survey

    Time frame: 3 months & 12 months

  20. Overall self-rated health status

    Measured using the EQ-5D 5 level version, specifically using the EQ visual analogue scale (EQ-VAS; range, 0-100; higher score indicates better self-rated health where 100 = best imaginable health state)

    Time frame: 3 months & 12 months

  21. Well-being score

    Measured using the World Health Organization (Five) Well-Being Index (raw score is calculated from totalling 5 items and is converted to a percentage score when multiplied by 4; percentage score range, 0-100; higher score indicates better better quality of life where 100 represents best possible quality of life)

    Time frame: 3 months & 12 months

  22. Social connectedness score

    Measured using the Duke Social Support Index (total score range, 11-33; higher values indicate higher levels of support)

    Time frame: 3 months & 12 months

  23. Sleep quality global score

    Measured using the Pittsburgh Sleep Quality Index (calculated by totalling the sum of 7 component scores; score range, 0-21; higher scores indicate worse sleep quality)

    Time frame: 3 months & 12 months

07

Study locations

40 sites
  • Dort Federal Credit Union Event Center
    Flint, Michigan 48503, United States
  • Saginaw Valley State University
    Saginaw, Michigan 48710, United States
  • Veterans Memorial Coliseum
    Portland, Oregon 97227, United States
  • City of Brooks
    Brooks, Alberta, Canada
  • Mount Royal University
    Calgary, Alberta, Canada
  • University of Lethbridge
    Lethbridge, Alberta T1K 3M4, Canada
  • Downtown Medicine Hat YMCA
    Medicine Hat, Alberta T1A 3A9, Canada
  • Northside Community Centre YMCA of Northern Alberta
    Red Deer, Alberta T4P 3E9, Canada
  • Club XO Fitness
    Chilliwack, British Columbia V2P 8G1, Canada
  • YMCA Kamloops
    Kamloops, British Columbia V2C 2L7, Canada
  • YMCA Okanagan
    Kelowna, British Columbia V1Y 6V8, Canada
  • YMCA-YWCA Westhills
    Langford, British Columbia V9B 0S2, Canada
  • Langley Events Centre
    Langley, British Columbia V2Y 3J4, Canada
  • Penticton Community Centre
    Penticton, British Columbia V2A 7K9, Canada
  • YMCA of Northern BC
    Prince George, British Columbia V2L 4V7, Canada
  • Shaw Centre
    Salmon Arm, British Columbia V1E 2S4, Canada
  • Avenir Centre
    Moncton, New Brunswick E1C 0V2, Canada
  • Afterburn Performance
    Saint John, New Brunswick E2J 1A2, Canada
  • YMCA of Halifax and Dartmouth
    Halifax, Nova Scotia B3J 1L2, Canada
  • Barrie YMCA
    Barrie, Ontario L4N 1M7, Canada
  • YMCA of Central Eastern Ontario - Belleville Branch
    Belleville, Ontario K8N 2G1, Canada
  • Les Chater Family YMCA
    Hamilton, Ontario L8P 2Z1, Canada
  • YMCA of Kingston
    Kingston, Ontario K7L 4T9, Canada
  • A.R. Kaufman Family YMCA
    Kitchener, Ontario N2G 3C5, Canada
  • Bostwick YMCA
    London, Ontario N6K 3X4, Canada
  • Mississauga Burnhamthorpe Rd. YMCA Centre
    Mississauga, Ontario L5B 3R2, Canada
  • YMCA of North Bay
    North Bay, Ontario P1B 6G2, Canada
  • Oshawa Mary Street YMCA Centre
    Oshawa, Ontario L1G 8C1, Canada
  • YMCA of Owen Sound Grey Bruce
    Owen Sound, Ontario N4K 0C6, Canada
  • Balsillie Family YMCA
    Peterborough, Ontario K9J 3H8, Canada
  • YMCA Jerry McCaw Family Centre
    Sarnia, Ontario N7S 6G5, Canada
  • YMCA of Sault Ste Marie
    Sault Ste Marie, Ontario P6B 1Y3, Canada
  • Walker Family YMCA
    St. Catharines, Ontario L2N 7P9, Canada
  • YMCA Sudbury
    Sudbury, Ontario P3E 3M7, Canada
  • YMCA at Central Park Athletics
    Windsor, Ontario N7G 4H5, Canada
  • University of Prince Edward Island
    Charlottetown, Prince Edward Island C1A 4P3, Canada
  • CBI Health Centre
    Prince Albert, Saskatchewan S6W 1A1, Canada
  • University of Regina
    Regina, Saskatchewan S4S 0A2, Canada
  • YMCA of Saskatoon
    Saskatoon, Saskatchewan S7K 0C7, Canada
  • Lt. Colonel Clifton Centre
    Swift Current, Saskatchewan S9H 3W1, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 7, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03636282
Lead sponsor
Western University, Canada
Collaborators
Canadian Institutes of Health Research (CIHR), Public Health Agency of Canada (PHAC)
Responsible party
Robert Petrella (Professor, Western University, Canada) — Principal investigator
First posted
Aug 17, 2018
Start date
Nov 13, 2018
Primary completion
Nov 28, 2022
Completion
May 3, 2023
Last update
Jun 7, 2023

Study contacts

Robert Petrella, MD, PhD
principal investigator · Western University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2023. You cannot join it, but the record below documents what was studied.

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