Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for not_applicable chronic-pain

Timeline
31mo left

Started Oct 2026

Typical duration for not_applicable chronic-pain

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 12, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

May 27, 2026

Completed
4 months until next milestone

Study Start

First participant enrolled

October 1, 2026

Expected
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2029

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2029

Last Updated

May 27, 2026

Status Verified

May 1, 2026

Enrollment Period

2.6 years

First QC Date

May 12, 2026

Last Update Submit

May 19, 2026

Conditions

Keywords

web-based health promotion

Outcome Measures

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

    Each Mission lasts 6-12 weeks

Secondary Outcomes (5)

  • Impact of the Online Wellness Missions on Body Weight

    Each intervention lasts 6-12 weeks

  • Change in Sleep Quality and Chronic Pain

    Each Mission lasts between 6 and 12 weeks

  • Change in Stress Level

    Each intervention lasts 6-12 weeks

  • Change in Perceived Social Isolation

    Each Mission lasts 6-12 weeks

  • Login Days

    Each Mission lasts between 6 and 12 weeks.

Study Arms (1)

online web-based health promotion

EXPERIMENTAL

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.

Behavioral: Online Web-based Health Promotion

Interventions

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.

online web-based health promotion

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Canadian Woman Veteran or
  • Family Member of a Canadian Women Veteran or
  • Friend of a Canadian Women Veteran

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Chronic PainSocial IsolationSedentary Behavior

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsSocial BehaviorBehavior

Study Officials

  • Steven Grover, MD

    McGill University Health Centre/Research Institute of the McGill University Health Centre

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Steven Grover, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Investigator

Study Record Dates

First Submitted

May 12, 2026

First Posted

May 27, 2026

Study Start (Estimated)

October 1, 2026

Primary Completion (Estimated)

May 1, 2029

Study Completion (Estimated)

May 1, 2029

Last Updated

May 27, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Participants are assured that their confidential individual health data will not be shared with anyone else.