- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT03059199
HAT TRICK: An Innovative Health Promotion Program for Men
30 de outubro de 2018 atualizado por: 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.
Visão geral do estudo
Status
Concluído
Condições
Intervenção / Tratamento
Descrição detalhada
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.
Tipo de estudo
Intervencional
Inscrição (Real)
61
Estágio
- Não aplicável
Contactos e Locais
Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.
Locais de estudo
-
-
British Columbia
-
Kelowna, British Columbia, Canadá
- Prospera Place
-
-
Critérios de participação
Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.
Critérios de elegibilidade
Idades elegíveis para estudo
35 anos e mais velhos (Adulto, Adulto mais velho)
Aceita Voluntários Saudáveis
Sim
Gêneros Elegíveis para o Estudo
Macho
Descrição
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
Plano de estudo
Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Prevenção
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
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.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Program Feasibility
Prazo: 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)
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Dietary Behaviour
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
|
Colaboradores e Investigadores
É aqui que você encontrará pessoas e organizações envolvidas com este estudo.
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Cristina Caperchione, PhD, UBCO Health and Exercise Sciences
Publicações e links úteis
A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.
Publicações Gerais
- 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.
Datas de registro do estudo
Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.
Datas Principais do Estudo
Início do estudo (Real)
20 de outubro de 2016
Conclusão Primária (Real)
22 de junho de 2018
Conclusão do estudo (Real)
22 de junho de 2018
Datas de inscrição no estudo
Enviado pela primeira vez
18 de novembro de 2016
Enviado pela primeira vez que atendeu aos critérios de CQ
16 de fevereiro de 2017
Primeira postagem (Real)
23 de fevereiro de 2017
Atualizações de registro de estudo
Última Atualização Postada (Real)
1 de novembro de 2018
Última atualização enviada que atendeu aos critérios de controle de qualidade
30 de outubro de 2018
Última verificação
1 de outubro de 2018
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- H1600736
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
NÃO
Descrição do plano IPD
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.
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
Ensaios clínicos em Prevenção do Câncer
-
Sohag UniversityInscrevendo-se por convite
-
Turku University HospitalLounais-Suomen SyöpäyhdistysAinda não está recrutandoSobrevivente de cancerFinlândia
-
Istanbul Aydın UniversityConcluído
-
Roswell Park Cancer InstituteNational Cancer Institute (NCI)RetiradoSobrevivente de cancerEstados Unidos
-
University of Alabama at BirminghamNational Cancer Institute (NCI); Auburn UniversityConcluído
-
Rutgers, The State University of New JerseyNational Cancer Institute (NCI)ConcluídoSobrevivente de cancerEstados Unidos
-
Wake Forest University Health SciencesNational Cancer Institute (NCI)ConcluídoSobrevivente de cancerEstados Unidos, Guam
-
Wake Forest University Health SciencesNational Cancer Institute (NCI); National Institute of Mental Health (NIMH)ConcluídoSobrevivente de cancerEstados Unidos
-
Masonic Cancer Center, University of MinnesotaConcluídoSobrevivente de cancerEstados Unidos
-
Abramson Cancer Center of the University of PennsylvaniaConcluídoPlano de cuidados de sobrevivência LIVESTRONG: coleta contínua de dados e pesquisa de acompanhamentoPaciente com cancerEstados Unidos