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Behavioral Intervention
Healthy Lifestyle Intervention for Obesity in Teens (LIFT Trial)
N/A
Recruiting
Led By Sarah E Messiah, Ph.D., MPH
Research Sponsored by The University of Texas Health Science Center, Houston
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must meet National Institutes of Health criteria to qualify for MBS for adolescents (BMI >35 kg/m2 and at least one existing co-morbidity [e.g. elevated blood pressure, hypercholesterolemia, etc.] or a BMI>40kg/m2).
Must meet National Institutes of Health criteria to qualify for MBS for adolescents (BMI >35 kg/m2 and at least one existing co-morbidity [e.g. elevated blood pressure, hypercholesterolemia, etc.] or a BMI>40kg/m2)
Must not have
Refuses to participate in the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month pre surgery and 6 months post surgery
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if combining weight-loss surgery with healthy living advice works well for teenagers who need extra help losing weight.
Who is the study for?
This trial is for teens with severe obesity, defined as having a BMI over 35 with related health issues like high blood pressure or cholesterol, or a BMI over 40. They must be considered candidates for bariatric surgery according to NIH guidelines and have received psychological clearance.
What is being tested?
The study tests a healthy lifestyle behavioral intervention supported by Metabolic and Bariatric Surgery (MBS) teams. It aims to see if this approach is feasible, acceptable, and effective in helping obese adolescents and their families make positive changes.
What are the potential side effects?
Since the intervention involves lifestyle changes rather than medication or invasive procedures, side effects may include typical challenges associated with diet change such as mood swings or fatigue but are generally minimal compared to medical interventions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am eligible for weight loss surgery based on my BMI and health conditions.
Select...
I am eligible for weight loss surgery based on my BMI and health conditions.
Select...
I have been cleared by a psychologist for surgery.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not want to participate in the study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 month pre surgery and 6 months post surgery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 month pre surgery and 6 months post surgery
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Health-related quality of life as measured by the HRQOL-14
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: TreatmentExperimental Treatment1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Metabolic and bariatric surgery, such as gastric bypass or sleeve gastrectomy, primarily work by reducing the stomach's size, which limits food intake and alters gut hormones to promote satiety and improve insulin sensitivity. These surgeries can lead to significant weight loss and remission of obesity-related conditions like type 2 diabetes.
When combined with behavioral strategies, such as dietary therapy, physical activity, and psychological support, the effectiveness of these surgeries is enhanced. This comprehensive approach helps patients maintain weight loss, adopt healthier lifestyles, and improve overall metabolic health, making it a crucial intervention for long-term obesity management.
Post-operative behavioural management in bariatric surgery: a systematic review and meta-analysis of randomized controlled trials.
Post-operative behavioural management in bariatric surgery: a systematic review and meta-analysis of randomized controlled trials.
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Who is running the clinical trial?
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,047 Previous Clinical Trials
2,731,037 Total Patients Enrolled
The University of Texas Health Science Center, HoustonLead Sponsor
944 Previous Clinical Trials
344,449 Total Patients Enrolled
Sarah E Messiah, Ph.D., MPHPrincipal InvestigatorThe University of Texas Health Science Center, Houston
Media Library
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.
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