N/A
N=13
Wellness Achieved Through Changing Habits (The WATCH Study)
Weight Loss · Obesity · Overweight
Bottom Line
View on ClinicalTrials.gov: NCT03284788 ↗Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Oct 2023
Primary outcome: Primary: Number of Participants Recruited — 16 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- ABT Weight Loss Intervention (Behavioral)
- Age
- Pediatric, Adult · 14+ yrs
- Sex
- Female
- Sponsor
- University of Florida
- Primary completion
- Jul 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants Recruited |
16 | — |
| PRIMARY Percentage of Participants Who Did Not Complete the Intervention. |
15.4 | — |
| PRIMARY Percentage of Participants Who Decide to Participate in the Intervention |
81.3 | — |
| PRIMARY Percentage of Participants Who Attend All Intervention Sessions. |
90.9 | — |
| SECONDARY Change in BMI Z-score |
-0.15 | — |
Summary
The purpose of this pilot, feasibility study is to investigate the acceptability of an acceptance-based therapy healthy lifestyle intervention in adolescent girls with overweight/obesity.
Eligibility Criteria
Inclusion Criteria
- Adolescent girls between ages 14-19 with overweight or obesity above the 85th percentile for sex and age as determined by CDC growth charts
Exclusion Criteria
- Known pregnancy or plans to become pregnant in the next 2 years
- Any condition prohibiting physical activity
- A diagnosis of cardiovascular disease or diabetes
- Have active cancer or cancer requiring treatment in the past 2 years
- Have active or chronic infections (e.g., HIV or TB)
- Have active kidney disease or lung disease
- An eating disorder or substance abuse disorder
- Having begun a course of or changed the dosage of any medications known to affect appetite or body composition within the previous 3 months
- Weight loss greater than or equal to 5% in the previous 6 months
- If they do not follow the study plan
Data sourced from ClinicalTrials.gov (NCT03284788). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.