跳至主要内容
临床试验/NCT03611829
NCT03611829终止不适用

An ACT-Based Physician-Delivered Weight Loss Intervention

McGill University0 个研究点目标入组 87 人开始时间: 2016年5月7日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
87
主要终点
Emotional Eating Change

研究概览

简要总结

The purpose of the present study was to conduct a pilot RCT to test the feasibility of a physician-delivered ACT-based intervention for emotional eaters with overweight/obesity against standard care at a network of weight loss clinics. Participants were randomized to receive either standard care at the clinics or the ACT intervention.

详细描述

The purpose of the present study was to conduct a pilot RCT to test the feasibility of a physician-delivered ACT-based intervention for emotional eaters with overweight/obesity against standard care at a network of weight loss clinics. Psychology clinical PhD students trained physicians in the delivery of the brief manualized intervention and were available for regular consults. The intervention consisted of eight, 5-10 minute sessions that could be easily incorporated into the physician's current practice. Over the duration of the ACT intervention, physicians met individually with patients to teach them various techniques to address and improve mindfulness, acceptance, and values clarification and commitment, all of which emotional eaters have been found to struggle with (Forman & Butryn, 2014). The proven habit formation technique of if-then planning (Gollwitzer, 1993) was used throughout these sessions in order to train emotional eaters to habitually use ACT techniques and to change the maladaptive habit of eating in response to negative emotions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Participants were blind to their condition, but physicians and administrative staff were not blind to participant condition. Physicians were not blind to participant condition because they were responsible for delivering the ACT intervention or standard care. They were thus required to know the participant's condition in order to deliver the adequate treatment. Administrative staff was responsible for providing physicians with this information and organizing study paperwork and thus needed to be aware of participant condition as well.

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

  • Only participants considered to be emotional eaters, as assessed by a score of 3.25 or higher on the Dutch Eating Behavior Questionnaire (DEBQ), were recruited for the study (van Strien, Herman, Anschutz, Engels, & de Weerth, 2012).

排除标准

  • Not being an emotional eater.
  • Participants who did not speak, write, and read in English fluently were excluded from the study, as well as those who were pregnant.

结局指标

主要结局

Emotional Eating Change

时间窗: Baseline to Post-Intervention (on average, 16 weeks)

Assessed by the Dutch Eating Behavior Questionnaire (DEBQ) emotional eating subscale. Scores range from 1 (never) to 5 (very often). Lower scores reflect lower emotional eating. This subscale score is calculated by taking the mean of all items on the subscale. Negative change scores reflect decreases in emotional eating.

Weight Change

时间窗: Baseline to Post-Intervention (on average, 16 weeks)

Weight change in kilograms

次要结局

  • Restraint Eating Change(Baseline to Post-Intervention (on average, 16 weeks))
  • Distress Tolerance Change(Baseline to Post-Intervention (on average, 16 weeks))
  • Values Clarification/ACT Application Change(Baseline to Post-Intervention (on average, 16 weeks))
  • Body Fat Percentage Change(Baseline to Post-Intervention (on average, 16 weeks))
  • External Eating Change(Baseline to Post-Intervention (on average, 16 weeks))
  • Mindfulness Awareness Change(Baseline to Post-Intervention (on average, 16 weeks))

研究者

申办方类型
Other
责任方
Sponsor

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