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Dyadic Interventions for Obesity (DATE Trial)
N/A
Waitlist Available
Research Sponsored by Concordia University, Montreal
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Obesity: BMI between 30-45 kg/m2
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 4 months, 7 months, 16 months
Awards & highlights
DATE Trial Summary
This trial will study how well a health behavior change intervention works for obese older adults who are in a relationship.
Who is the study for?
The DATE study is for older adult couples dealing with obesity, where at least one partner is retired and they've been living together for over two years. They must have a BMI between 30-45 but can't join if they've had a stroke, heart issues, uncontrolled diabetes, are on special diets or weight loss programs, or have other medical conditions preventing physical activity.Check my eligibility
What is being tested?
This trial tests a new way to help obese couples eat better and exercise more by working together. It compares a 'dyadic health behaviour change intervention'—where partners support each other—to just getting nutrition advice. The goal is to see if this team approach helps create a home that supports healthy habits.See study design
What are the potential side effects?
Since the interventions involve lifestyle changes like diet and exercise rather than medication, typical drug side effects aren't expected. However, participants may experience muscle soreness from increased physical activity or digestive changes due to diet adjustments.
DATE Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My BMI is between 30 and 45.
DATE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 4 months, 7 months, 16 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 4 months, 7 months, 16 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Healthy Eating Index
Secondary outcome measures
Change in Autonomy Support
Change in Communal Coping
Change in Dyadic Coping
+7 moreOther outcome measures
Changes in Action Planning
Changes in Depressive Symptoms
Changes in Functional Fitness
+4 moreDATE Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Dyadic Health Behaviour Change InterventionExperimental Treatment1 Intervention
The dyadic health behaviour change intervention is a 10 sessions program provided over 16 weeks. It includes nutritional, physical activity and sedentary related information, as well as couples-based adaptation of motivational interviewing, self-monitoring, goals setting, stimulus control, problem-solving, and relapse prevention as well as specific strategies to support their partner's autonomy and intrinsic motivation.
Group II: Dyadic nutrition counselling interventionActive Control1 Intervention
The couples-based nutrition counselling intervention is a 10 sessions program provided over 16 weeks. Topics are based on Dietitians of Canada's Practice-based Evidence in Nutrition discussions. Participants are also encouraged to meet the current physical activity recommendations. Both members of the couples are seen at the same, but no intervention target specifically the behaviour change process or the romantic relationship.
Find a Location
Who is running the clinical trial?
Concordia University, MontrealLead Sponsor
22 Previous Clinical Trials
4,597 Total Patients Enrolled
Centre de Recherche de l'Institut Universitaire de Geriatrie de MontrealOTHER
22 Previous Clinical Trials
8,819 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- One of us is retired.I have no health issues stopping me from doing physical activities.I have had a stroke.You have an eating disorder.My BMI is between 30 and 45.My diabetes is not under control.You are currently participating in a program to lose weight.You are following a specific diet plan.I have had heart problems or surgery related to my heart.
Research Study Groups:
This trial has the following groups:- Group 1: Dyadic Health Behaviour Change Intervention
- Group 2: Dyadic nutrition counselling intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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