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Bariatric Surgery Study (SIBS)

2018年12月4日 更新者:Jonathan Kanter、University of Washington

A Social Functioning Intervention to Target Depression Post Bariatric Surgery

The current study proposes an open clinical trial to investigate the effectiveness of a social functioning intervention on bariatric surgery outcomes and depression. The treatment will be administered in a group format over 10 weekly/biweekly sessions and will take place at the University of Washington Weight Loss Management Clinic (WLMC) at the Roosevelt Clinic location. Effects of the intervention will be measured with self-report questionnaires and by self-report of behaviors outside of assessment sessions (via questionnaires and self-report of adherence to treatment). Data collection will occur at specific time points including before treatment, after treatment, and two months after treatment.

研究概览

详细说明

As of 2009, 344,000 bariatric procedures were performed annually . Although some studies report depressive symptoms decrease in the 6 months after bariatric surgery, there is growing body of literature suggesting there exists a subgroup of patients whose depressive symptoms worsen after surgery and the likelihood of developing depressive symptoms increases longitudinally. Depression can be an indicator of an increased risk of self-harm and additional studies have found that the risk of suicide may increase post bariatric surgery compared to obese individuals who have not undergone surgery.

Research supports that psychosocial factors contribute to successful postoperative outcomes. Functional Analytic Psychotherapy shows potential to impact social variables that may be relevant to bariatric surgery outcomes including depression. In this context, FAP aims to improve interpersonal relationships through experientially teaching skills intended to increase social connection. FAP also seeks to increase awareness, which includes the ability to view interpersonal interactions from multiple perspectives, allowing new interpersonal skills to emerge.

The present study seeks to evaluate the use of a FAP group to enhance interpersonal relating with a sample of post-bariatric surgery patients. Measures will be collected on quality of life and variables involved in interpersonal connectedness.

研究类型

介入性

注册 (预期的)

20

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Washington
      • Seattle、Washington、美国、98105
        • Weight Loss Management Center at UWMC-Roosevelt

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Older than 18
  • Speak English as a primary language
  • Had Bariatric Surgery in the past 6-24 months (bypasses (Roux-en-Y) or sleeves)
  • Yes to one or both of the first two PHQ-9 Questions
  • Not pregnant
  • Not traveling anywhere in the next 6 months
  • No surgeries scheduled in the next 12 months

Exclusion Criteria:

• No exclusion criteria are utilized in the present study.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:FAP Intervention Group
All of the clients in the FAP intervention group will begin treatment at the same time and complete 3 assessments.
The intervention itself is based on the procedures of Functional Analytic Psychotherapy, a behavioral intervention focusing on improving social functioning.
无干预:Control Group
The clients in the control group will take their assessments at the same time as those in the FAP intervention group.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Patient Health Questionnaire-9 (PHQ-9)
大体时间:Baseline
based directly on the nine diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual Diploma in Social Medicine-IV
Baseline
Patient Health Questionnaire-9 (PHQ-9)
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
based directly on the nine diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual Diploma in Social Medicine-IV
Post Intervention (Approximately 12 Weeks from Baseline)
Patient Health Questionnaire-9 (PHQ-9)
大体时间:Follow Up (3 Months after Intervention)
based directly on the nine diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual Diploma in Social Medicine-IV
Follow Up (3 Months after Intervention)

次要结果测量

结果测量
措施说明
大体时间
World Health Organization Quality of Life
大体时间:Baseline
a measure of an individual's physical health, psychological state, personal beliefs, social relationships and their relationship to salient features of their environment.
Baseline
World Health Organization Quality of Life
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
a measure of an individual's physical health, psychological state, personal beliefs, social relationships and their relationship to salient features of their environment.
Post Intervention (Approximately 12 Weeks from Baseline)
World Health Organization Quality of Life
大体时间:Follow Up (3 Months after Intervention)
a measure of an individual's physical health, psychological state, personal beliefs, social relationships and their relationship to salient features of their environment.
Follow Up (3 Months after Intervention)
Drug Abuse Screening Test
大体时间:Baseline
a sensitive screening instrument for the abuse of drugs other than alcohol
Baseline
Drug Abuse Screening Test
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
a sensitive screening instrument for the abuse of drugs other than alcohol
Post Intervention (Approximately 12 Weeks from Baseline)
Drug Abuse Screening Test
大体时间:Follow Up (3 Months after Intervention)
a sensitive screening instrument for the abuse of drugs other than alcohol
Follow Up (3 Months after Intervention)
Paffenbarger Physical Activity Questionnaire
大体时间:Baseline
asks participants about their current and previous exercise habits
Baseline
Paffenbarger Physical Activity Questionnaire
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
asks participants about their current and previous exercise habits
Post Intervention (Approximately 12 Weeks from Baseline)
Paffenbarger Physical Activity Questionnaire
大体时间:Follow Up (3 Months after Intervention)
asks participants about their current and previous exercise habits
Follow Up (3 Months after Intervention)
Proximal Change Variables
大体时间:Baseline
assesses participant's eating habits as well as tobacco and alcohol use
Baseline
Proximal Change Variables
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
assesses participant's eating habits as well as tobacco and alcohol use
Post Intervention (Approximately 12 Weeks from Baseline)
Proximal Change Variables
大体时间:Follow Up (3 Months after Intervention)
assesses participant's eating habits as well as tobacco and alcohol use
Follow Up (3 Months after Intervention)
Weight Control Questionnaire
大体时间:Baseline
asks participants to report if they have ever used any weight control practices
Baseline
Weight Control Questionnaire
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
asks participants to report if they have ever used any weight control practices
Post Intervention (Approximately 12 Weeks from Baseline)
Weight Control Questionnaire
大体时间:Follow Up (3 Months after Intervention)
asks participants to report if they have ever used any weight control practices
Follow Up (3 Months after Intervention)
Fear of Intimacy Scale (FIS)
大体时间:Baseline
The FIS is a 35 item measure of self-disclosure, social intimacy, and social desirability. All items are scored on a 5-point Likert scale
Baseline
Fear of Intimacy Scale (FIS)
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
The FIS is a 35 item measure of self-disclosure, social intimacy, and social desirability. All items are scored on a 5-point Likert scale
Post Intervention (Approximately 12 Weeks from Baseline)
Fear of Intimacy Scale (FIS)
大体时间:Follow Up (3 Months after Intervention)
The FIS is a 35 item measure of self-disclosure, social intimacy, and social desirability. All items are scored on a 5-point Likert scale
Follow Up (3 Months after Intervention)
Social Support Survey
大体时间:Baseline
provides an assessment of several domains of social support including tangible support, emotional support, affective support, and positive support
Baseline
Social Support Survey
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
provides an assessment of several domains of social support including tangible support, emotional support, affective support, and positive support
Post Intervention (Approximately 12 Weeks from Baseline)
Social Support Survey
大体时间:Follow Up (3 Months after Intervention)
provides an assessment of several domains of social support including tangible support, emotional support, affective support, and positive support
Follow Up (3 Months after Intervention)
University of California, Los Angeles Loneliness Scale
大体时间:Baseline
designed to measure one's subjective feelings of loneliness as well as feelings of social isolation
Baseline
University of California, Los Angeles Loneliness Scale
大体时间:Post Intervention (Approximately 12 Weeks from Baseline)
designed to measure one's subjective feelings of loneliness as well as feelings of social isolation
Post Intervention (Approximately 12 Weeks from Baseline)
University of California, Los Angeles Loneliness Scale
大体时间:Follow Up (3 Months after Intervention)
designed to measure one's subjective feelings of loneliness as well as feelings of social isolation
Follow Up (3 Months after Intervention)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2019年1月1日

初级完成 (预期的)

2019年6月1日

研究完成 (预期的)

2019年12月1日

研究注册日期

首次提交

2018年11月27日

首先提交符合 QC 标准的

2018年12月4日

首次发布 (实际的)

2018年12月6日

研究记录更新

最后更新发布 (实际的)

2018年12月6日

上次提交的符合 QC 标准的更新

2018年12月4日

最后验证

2018年12月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • STUDY00005196

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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