Intensive Longitudinal Assessment of Stress and Stress-related Concepts Across a Behavioral Weigh… (NCT06668259) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Intensive Longitudinal Assessment of Stress and Stress-related Concepts Across a Behavioral Weight Loss Intervention
United States52 participantsStarted 2025-06-20
Plain-language summary
Examine the association between variability in individual stress and related concepts with weight loss, physical activity, and sleep across a behavioral weight loss program
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Enrolled in a community-based weight loss program centered in a metropolitan area of a Midwest state. Based on this criteria, we will anticipate participants are greater than 18 years of age, and have obesity.
* Must own a smart phone and be willing to download the mobile application to receive text messages
Exclusion Criteria:
* Report a current medical condition or treatment for a medical condition that could affect body weight.
* Current psychological condition (including clinically diagnosed depression) that is untreated, hospitalization for a psychological condition within the past 12 months, or not being on a stable dose of treatment for at least 6 months.
* Is not fluent in writing or speaking the English language.
* Mobility limitations so they are unable to perform physical activity.
* Family member currently enrolled in the study or has a family member that previously participated in the study.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Weight (kg)
Timeframe: 0 Weeks, 6 Weeks, 12 Weeks, and 26 Weeks
2
Physical Activity
Timeframe: 0 Weeks, 6 Weeks, 12 Weeks, and 26 Weeks
3
Sleep
Timeframe: 0 Weeks, 6 Weeks, 12 Weeks, and 26 Weeks
4
Stress-related Concepts (EMA)
Timeframe: 0 Weeks, 6 Weeks, 12 Weeks, and 26 Weeks