The Women Veteran's Health Mission

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMcGill University Health Centre/Research Institute of the McGill University Health Centre

About this trial

The purpose of this study is to evaluate the impact of a customized web-based e-health program to provide online health promotion (Missions), peer support, and social connectivity to women Veterans and their families.

Primary Objective

• To assess participant engagement in the program including:

completion rates (%) for each 6-12 week health program (Mission) defined as completing the assessments following the intervention number of login days among those who register and drop-out rates (%) defined as those who start but do not complete the program.

Secondary Objectives • To assess the impact of a web-based wellness program on health metrics including: change in body weight (lbs) sleep, and chronic pain (PROMIS 29 Questionnaire) stress (PROMIS Perceived Stress) social isolation (PROMIS Social Isolation Short Form 4a).

• To determine whether there is a dose-response between the number of login days into the program and changes in health metrics.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Canadian Woman Veteran or

Family Member of a Canadian Women Veteran or

Friend of a Canadian Women Veteran

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Online Web-based Health Promotion

    Behavioral

    Online web-based health promotion program to increase physical activity. Participants will also learn and practice other healthy lifestyle habits to improve physical and mental health.

Treatment groups

500 Participants
are divided into 1 treatment group
Group A: online web-based health promotionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Program Completion Rates

Program completion rates (%) for each 6-12 week health program (Mission) defined as completing the assessments at baseline and following the 6-12 week intervention

Time frame
Each Mission lasts 6-12 weeks

Secondary outcomes

1

Impact of the Online Wellness Missions on Body Weight

change in body weight (lbs) between baseline and completion of the intervention

Time frame
Each intervention lasts 6-12 weeks
2

Change in Sleep Quality and Chronic Pain

Change in sleep quality and chronic pain (PROMIS 29 Questionnaire) measured at baseline and following completion of the intervention (Mission)

Time frame
Each Mission lasts between 6 and 12 weeks
3

Change in Stress Level

Change in stress level (PROMIS Perceived Stress scale) between baseline and completion of intervention

Time frame
Each intervention lasts 6-12 weeks
4

Change in Perceived Social Isolation

Change in Perceived Social isolation (PROMIS Social Isolation Short Form 4a) between baseline and completion of intervention (Mission).

Time frame
Each Mission lasts 6-12 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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