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HAT TRICK: An Innovative Health Promotion Program for Men

30 oktober 2018 uppdaterad av: 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.

Studieöversikt

Status

Avslutad

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

61

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • British Columbia
      • Kelowna, British Columbia, Kanada
        • Prospera Place

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

35 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Manlig

Beskrivning

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

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Program Feasibility
Tidsram: 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)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Dietary Behaviour
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

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

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

20 oktober 2016

Primärt slutförande (Faktisk)

22 juni 2018

Avslutad studie (Faktisk)

22 juni 2018

Studieregistreringsdatum

Först inskickad

18 november 2016

Först inskickad som uppfyllde QC-kriterierna

16 februari 2017

Första postat (Faktisk)

23 februari 2017

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

1 november 2018

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

30 oktober 2018

Senast verifierad

1 oktober 2018

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • H1600736

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

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.

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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