跳至主要内容
临床试验/NCT07406568
NCT07406568Enrolling By Invitation不适用

Pilot Trial of the Move Healthier Group

Dartmouth-Hitchcock Medical Center1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2026年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
12
试验地点
1
主要终点
Objective physical activity

研究概览

简要总结

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.

详细描述

Individuals seeking weight loss are often encouraged to increase their exercise engagement as a health-promoting behavior. However, exercise engagement is often connected directly to caloric intake within weight loss interventions, so it is likely that individuals seeking weight loss are engaging in some level of compensatory exercise even in the absence of other disordered eating symptoms. Compensatory exercise is defined as exercising to "offset" or "make up for" calories consumed with the intent of controlling one's body weight or shape. The researchers are developing a new group to promote healthy exercise and are interested in studying whether this group helps people increase their exercise without increasing risk for compensatory exercise or other disordered eating behaviors.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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)

排除标准

  • 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.

研究组 & 干预措施

Move Healthier Group Intervention Arm

Experimental

This group-based intervention aims to promote healthy exercise without increasing risk for compensatory exercise or other disordered eating behaviors. Participants will attend 8 weekly 90-minute group intervention sessions via telehealth software.

干预措施: Move Healthier Intervention (Behavioral)

结局指标

主要结局

Objective physical activity

时间窗: From enrollment to the end of treatment at 12 weeks

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.

Self-reported physical activity

时间窗: From enrollment to the end of treatment at 12 weeks

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.

Eating disorder symptoms

时间窗: Baseline and post-intervention (week 12)

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.

次要结局

  • Weight bias internalization(baseline and post-intervention (week 12))
  • intervention acceptability(post-intervention (week 12))
  • intervention feasibility(post-intervention (week 12))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Elizabeth.W.Lampe

Clinical Psychology Fellow, Weight Center

Dartmouth-Hitchcock Medical Center

研究点 (1)

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