Purpose After Service Through Sport (PASS) (NCT05289882) | Clinical Trial Compass
WithdrawnNot Applicable
Purpose After Service Through Sport (PASS)
Stopped: Unable to recruit sufficient sample to commence trial
Canada0Started 2022-09-01
Plain-language summary
The purpose of this study is to evaluate the efficacy of a gender-sensitized social-connectedness physical activity program in relation to key markers of well-being among military veteran men over 6 months.
Who can participate
SexALL
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Inclusion Criteria:
* Former members of the Canadian (or Allied Forces; e.g., NATO countries) military, or current members of the Canadian military, and not experience any contraindication which might prevent that person from participating in moderate-intensity physical activity.
* Self-identification as a man (if sex at birth is 'female' but participants identify as 'man' they are eligible to participate).
* Have received full dosage of the COVID-19 vaccination (min 2 injections) and must provide proof of vaccination, as this is required to access all active military bases in Canada.
* Be able to read and understand English or French.
* Have access to a computer, tablet, or other device, that has access to the internet.
* Live at, or in close proximity to, one of the nine study locations (Esquimalt, BC; Edmonton, AB, Shilo, MB; Borden, ON; Kingston, ON; Petawawa, ON; Valcartier, QC; Montreal, QC; Gagetown, NB)
Exclusion Criteria:
* Not a former member of the Canadian (or Allied Forces; e.g., NATO countries) military, or current member of the Canadian military.
* Unable to participate in moderate-intensity physical activity (as screened via the PAR-Q and ePARmedX), including a lack of ability to receive doctor's clearance for participating in physical activity.
* Unable to speak or read English or French
* Lack of internet access which prevents access to online materials (e.g., questionnaires).
* Participants do not self-identify as 'man'. If participants disclose 'sex' as…
What they're measuring
1
Change in well-being (psychological flourishing) over the course of the intervention
Timeframe: Tracked monthly for 6 months (baseline, followed by 6 months of intervention)