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HAT TRICK: An Innovative Health Promotion Program for Men

30 oktober 2018 bijgewerkt door: Cristina Caperchione, University of British Columbia

HAT TRICK: Examining the Feasibility of a Gender Sensitive Intervention Focused on Physical Activity, Healthy Eating and Connectedness in Male Hockey Fans

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.

Studie Overzicht

Toestand

Voltooid

Gedetailleerde beschrijving

Despite the benefits associated with lifestyle changes, men are less likely than women to engage in healthy lifestyle behaviours. Many men are reluctant and/or 'hard-to-reach', making it difficult to implement chronic illness prevention initiatives. Traditionally, a central challenge associated with engaging men in their health were perceptions that attention to one's health ran counter to masculine ideals of strength, self-reliance and independence. Thus, many men refrain from engaging in health promotion behaviors, such as PA and healthy eating. Research has highlighted the potential for professional sports teams/clubs to attract and engage men in healthy lifestyle behaviours. Such a strategy has been recognised as very powerful due to the traditional male environment within these clubs and the social-cultural connections the men often make with particular teams in terms of loyalty, identity and belonging. Thus, the purpose of this research is to develop and evaluate the feasibility of the HAT-TRICK Program, a gender-sensitive intervention program targeting PA, healthy eating and connectedness in men living in Kelowna, BC. This program will be delivered as a collaborative effort between the research team and the Kelowna Rockets, a major junior ice hockey team in Kelowna, BC. The Kelowna Rockets play in a centre with a capacity of over 6,000 and have one of the most loyal season ticket holders base in the Western Hockey League, with 4,500; the majority being men and between the ages of 40-70 years old. With assistance from the Rockets, participants (N=30) will be recruited via season ticket holders, at hockey games, though the Rockets webpage and local print and electronic media. Participants meeting all eligibility criteria will be invited to participate in the 12 week HAT-TRICK Program which will consist of a once a week, 90 minute combined physical activity (e.g., resistance training, "boot-camp" training, floor hockey, stair climbing) and health education session (e.g., goal setting, self-monitoring, barriers and benefits to PA, dealing with set-backs, healthy eating, alcohol consumption, etc.) to be held at the Kelowna Rockets game and training facility. Kelowna Rockets personnel (e.g., athletic therapist, nutritionist) and community experts (e.g., chef, fitness trainer) will be invited to lead some of the PA and nutrition sessions. Kelowna Rockets players will also visit the group during selected sessions to engage in the PA training with the men, further encouraging social support, connectedness and camaraderie. Primary (feasibility and acceptability) and secondary (PA, nutrition, quality of life, connectedness, anthropometrics) outcome measures will be evaluated using a mix-methods approach including; focus groups, self-reported questionnaires and objective physical activity and anthropometric methods. All measures will be collected at baseline, post-intervention (12 weeks) and at 9-month follow-up. Findings from the primary and secondary outcome measures will be used to refine the HAT-TRICK program in preparation for a full-scale evaluation (RCT). Innovative prevention and health promoting approaches are needed to better serve this 'hard to reach' population. This innovative program utilizes a gender sensitive approach to attract and engage men, providing them with a program that recognises their masculine values and interests. Furthermore, the collaborative (i.e., Kelowna Rockets) nature of this program is poised to reach a large proportion of men in the Okanagan by capitalizing on the social-cultural connections men often make with sports teams and using this as the lynchpin to engaging men in health behaviours.

Studietype

Ingrijpend

Inschrijving (Werkelijk)

61

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • British Columbia
      • Kelowna, British Columbia, Canada
        • Prospera Place

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

35 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Mannelijk

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Program Feasibility
Tijdsspanne: 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)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Dietary Behaviour
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Cristina Caperchione, PhD, UBCO Health and Exercise Sciences

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

20 oktober 2016

Primaire voltooiing (Werkelijk)

22 juni 2018

Studie voltooiing (Werkelijk)

22 juni 2018

Studieregistratiedata

Eerst ingediend

18 november 2016

Eerst ingediend dat voldeed aan de QC-criteria

16 februari 2017

Eerst geplaatst (Werkelijk)

23 februari 2017

Updates van studierecords

Laatste update geplaatst (Werkelijk)

1 november 2018

Laatste update ingediend die voldeed aan QC-criteria

30 oktober 2018

Laatst geverifieerd

1 oktober 2018

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • H1600736

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Beschrijving IPD-plan

Only the principal investigators and UBC research team members will have access to the raw data. CO-I's external to UBC will not require access to raw participant data. Any data that are shared will be aggregate data and have all identifiers removed. All of these individuals have training in issues concerning privacy, confidentiality, and are aware of their responsibilities to maintain these.

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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