Pilot Trial of the Move Healthier Group
1 other identifier
interventional
12
1 country
1
Brief Summary
The researchers are developing a new exercise-focused group and are interested in studying whether this group helps people increase their exercise without increasing risk for disordered eating behaviors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable obesity
Started Apr 2026
Shorter than P25 for not_applicable obesity
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 13, 2026
CompletedFirst Posted
Study publicly available on registry
February 12, 2026
CompletedStudy Start
First participant enrolled
April 16, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 30, 2026
April 28, 2026
April 1, 2026
5 months
January 13, 2026
April 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Objective physical activity
Objective physical activity will be measures as the total number of minutes per week of physical activity measured via Fitbit device worn during waking hours. The Fitbit data will yield a total count of the number of minutes of moderate-to-vigorous physical activity for each week during the intervention period, with higher counts indicating greater levels of activity.
From enrollment to the end of treatment at 12 weeks
Self-reported physical activity
Participants will also complete self-report measures of physical activity, including the International Physical Activity Questionnaire (IPAQ) and IPAQ-short form at group sessions and study assessments. The IPAQ asks patients to report on their total physical activity engagement over the past 7 days by light, moderate, and vigorous activity categories. The IPAQ yields a total count of the number of minutes of moderate-to-vigorous physical activity over the past week, with higher minutes indicating more activity.
From enrollment to the end of treatment at 12 weeks
Eating disorder symptoms
ED symptoms will be assessed via the Eating Disorder Examination Questionnaire (EDE-Q 6.0), which asks about ED symptoms over the past month (28 days). Compensatory exercise engagement will be assessed via an item asking, "Over the past 28 days, how many times have you exercised to "make up for" a binge-eating episode, and compulsive exercise will be assessed using the item "...how many times have you felt driven/compelled to exercise?" EDE-Q items are averages to calculate a total score ranging from 0-6, with higher scores indicating higher levels of eating pathology.
Baseline and post-intervention (week 12)
Secondary Outcomes (3)
Weight bias internalization
baseline and post-intervention (week 12)
intervention acceptability
post-intervention (week 12)
intervention feasibility
post-intervention (week 12)
Study Arms (1)
Move Healthier Group Intervention Arm
EXPERIMENTALThis group-based intervention aims to promote healthy exercise without increasing risk for compensatory exercise or other disordered eating behaviors. Participants will attend 12 weekly 90-minute group intervention sessions via telehealth software.
Interventions
The intervention aims to increase exercise using cognitive and behavioral skills integrated across several treatment manuals including the Physical Activity Cognitively Enhanced (PACE) intervention for healthy exercise promotion in eating disorders, acceptance-based and standard behavioral weight loss manuals, and affect-guided exercise prescriptions.
Eligibility Criteria
You may qualify if:
- Seen for weight loss treatment at DHMC Weight Center within the past year
- Speak, read, \& write English fluently
- Age 18 or older
- Appropriate for group visits (as assessed by referring provider)
You may not qualify if:
- Meets DSM-5 criteria for an eating disorder based on behavior frequencies reported on baseline EDE-Q
- Report contraindications for unsupervised physical activity on the PAR-Q, or have not been medically cleared by an MD for participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dartmouth-Hitchcock Clinics
Lebanon, New Hampshire, 03766, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Jessica Salwen-Deremer, PhD
Dartmouth Health
- PRINCIPAL INVESTIGATOR
Elizabeth Lampe, PhD
Dartmouth Health
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Clinical Psychology Fellow, Weight Center
Study Record Dates
First Submitted
January 13, 2026
First Posted
February 12, 2026
Study Start
April 16, 2026
Primary Completion (Estimated)
August 30, 2026
Study Completion (Estimated)
August 30, 2026
Last Updated
April 28, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share