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临床试验/NCT04867902
NCT04867902已完成不适用

Gaining Optimism After Weight Loss Surgery (GOALS) I: Proof-of-Concept Trial of a Positive Psychology-based Intervention to Increase Physical Activity After Bariatric Surgery

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2021年6月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
1
主要终点
Number of Intervention Sessions Completed

研究概览

简要总结

This study examines the feasibility, acceptability, and preliminary impact of an adapted positive psychology-motivational interviewing (PP-MI) intervention for physical activity among patients who have recently undergone bariatric surgery.

详细描述

This study will test a positive psychology-motivational interviewing (PP-MI) intervention for physical activity promotion in patients who have had bariatric surgery within the past 6-12 months. The investigators will enroll 12 participants. Study participation includes attending three study visits (two at baseline, one after the intervention) and receiving a 10-week physical activity intervention that includes once-weekly phone calls, a written manual, and a Fitbit activity tracker. Primary outcomes are feasibility and acceptability of the intervention and study procedures. Secondary outcomes include pre-post changes in physical activity and other psychological, behavioral, and physiological outcomes.

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
否

入选标准

  • •Adult (age 18+)
  • •History of bariatric surgery (gastric bypass or sleeve gastrectomy) at one of two academic medical centers within the past 6-12 months
  • •Interest in increasing physical activity
  • •Low physical activity, defined as <200 minutes/week self-reported moderate- to-vigorous physical activity
  • •Access to telephone for study sessions
  • •Able to read and speak English

排除标准

  • •Cognitive deficits precluding participation or informed consent
  • •Illness likely to lead to death in the next 6 months
  • •Inability to be physically active (e.g., severe arthritis)
  • •Participation in another program targeting physical activity besides their standard offerings at the surgery center.

研究组 & 干预措施

Positive Psychology-Motivational Interviewing Intervention

Experimental

Participants will receive a written treatment manual with detailed information about each topic. The intervention consists of 10 weekly phone sessions (30 minutes each). Each session includes a new psychological skill designed to increase positive emotions experienced during physical activity, a motivational skill designed to boost physical activity, and setting a physical activity goal for the next week using information from the Fitbit. A motivational interviewing approach will be used for all topics.

干预措施: Positive Psychology-Motivational Interviewing Intervention (Behavioral)

结局指标

主要结局

Number of Intervention Sessions Completed

时间窗: 10 weeks

Feasibility will be measured by examining the number of completed intervention sessions. The intervention will be considered feasible if at least 7/10 sessions are completed, on average.

Ease and Utility of Intervention Sessions

时间窗: 10 weeks

Acceptability will be measured with ratings of ease and utility after each exercise, measured on a 10-point Likert scale (1=very difficult/not at all helpful, 10=very easy/very helpful). The intervention will be considered acceptable if average ease and utility ratings are at least 7/10.

次要结局

  • Change in Systolic Blood Pressure(Baseline and 10-Week Follow-Up)
  • Change in Motivation to Change(Baseline and 10-Week Follow-Up)
  • Change in Exercise-specific Self-efficacy(Baseline and 10-Week Follow-Up)
  • Change in Steps(Baseline and 10-Week Follow-Up)
  • Change in Internalized Weight Bias(Baseline and 10-Week Follow-Up)
  • Change in Light Physical Activity(Baseline and 10-Week Follow-Up)
  • Change in Moderate to Vigorous Physical Activity (MVPA)(Baseline and 10-Week Follow-Up)
  • Change in Sedentary Time(Baseline and 10-Week Follow-Up)
  • Change in Optimism(Baseline and 10-Week Follow-Up)
  • Change in Depressive Symptoms(Baseline and 10-Week Follow-Up)
  • Change in Anxiety(Baseline and 10-Week Follow-Up)
  • Change in General Self-Efficacy(Baseline and 10-Week Follow-Up)
  • Change in Body Image(Baseline and 10-Week Follow-Up)
  • Change in Waist Circumference (in Centimeters)(Baseline and 10-Week Follow-Up)
  • Change in Body Composition(Baseline and 10-Week Follow-Up)
  • Change in A1C(Baseline and 10-Week Follow-Up)
  • Change in Exercise Identity(Baseline and 10-Week Follow-Up)
  • Change in Aerobic Capacity and Endurance(Baseline and 10-Week Follow-Up)
  • Change in High-density Lipoprotein (HDL)(Baseline and 10-Week Follow-Up)
  • Change in Inflammation(Baseline and 10-Week Follow-Up)
  • Change in Bariatric Surgery-specific Diet and Vitamin Adherence(Baseline and 10-Week Follow-Up)
  • Change in Body Weight(Baseline and 10-Week Follow-Up)
  • Change in Social Support for Eating Habits - Encouragement Subscale(Baseline and 10-Week Follow-Up)
  • Change in Self-Reported Physical Activity(Baseline and 10-Week Follow-Up)
  • Change in Social Support for Exercise(Baseline and 10-Week Follow-Up)

研究者

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

Emily Feig, Ph.D.

Instructor in Psychology

Massachusetts General Hospital

研究点 (1)

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