跳至主要内容
临床试验/NCT07212673
NCT07212673招募中不适用

Combining Digital Cognitive-behavior Therapy With Mindfulness Training for Binge Eating Disorder: a Feasibility Randomized Controlled Trial

Yeshiva University2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年11月2日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
2
主要终点
Feasibility / Completion (questionnaire developed by our lab)

研究概览

简要总结

The investigators will evaluate the acceptability and feasibility of a 16-session digital mindfulness-based and cognitive behavioral therapy (CBT) intervention for binge eating disorder (BED) + coached self-monitoring vs. a coached self-monitoring intervention. This study is a pilot randomized controlled trial.

详细描述

Procedures include completing: (1) pre-intervention screening assessment; (2) an initial baseline visit; (3) the assigned intervention; (4) a mid-study visit; (5) a post-intervention assessment (~18-weeks after baseline); and (6) a 2-month follow-up assessment.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age 18 years or older
  • ability to speak English fluently
  • meeting DSM-5 criteria for current BED (i.e., in the past three months)
  • willing and able to commit to the entire study protocol

排除标准

  • a BMI below 18.5
  • requiring immediate treatment for medical complications
  • having current anorexia or bulimia nervosa or purging behaviors within the past year
  • being pregnant or breast-feeding
  • experiencing other severe psychopathology or medical illness that would limit the participants' ability to comply with the demands of the current study (e.g. active suicidal risk, active psychotic disorder, unmedicated bipolar disorder, severe substance use disorder, cancer)
  • currently receiving BED or weight loss treatment (treatment for other conditions will be allowed, as long as the treatment is not mindfulness-based)
  • currently taking medications for weight loss, or beginning medications that affect eating/weight within the last six months.

结局指标

主要结局

Feasibility / Completion (questionnaire developed by our lab)

时间窗: From baseline to 2-month follow-up visit

Number of participants completing intervention

Acceptability

时间窗: After completing intervention, an average of 18-weeks

Dimensions of usability from the System Usability Scale; single-items measuring dimensions of acceptability, including overall satisfaction, engagement, visual appeal of content, understandability of program content, desire to continue the program, perceived skill acquisition, perceived confidence in implementing skills, and perceived helpfulness. Scores for each item range from 1 to 5, with higher scores indicating better acceptability. Scores will be averaged to obtain acceptability ratings.

次要结局

未报告次要终点

研究者

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

Margaret Sala

Assistant Professor

Yeshiva University

研究点 (2)

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