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临床试验/NCT00727675
NCT00727675已完成不适用

Chronic Pain and Opioid Dependence Assessment and Treatment

Yale University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2008年8月1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
15
试验地点
1
主要终点
Reduced illicit opioid use and pain

研究概览

简要总结

This study involves the development of an integrated psychotherapy that addresses both chronic pain and opioid dependence(POD).

详细描述

To conduct a pre-pilot study with 20 POD patients to a) evaluate the acceptability and potential efficacy of specific sessions (i.e., reduced illicit opioid use as assessed by urine toxicology and self-report findings, and decreased pain as evidenced by attenuated pain intensity and pain interference on self-report measures from baseline throughout treatment) for inclusion in integrated Cognitive Behavioral Therapy (CBT) for POD and the sequence of sessions, b) assess patients' satisfaction with integrated CBT as evidenced by qualitative feedback from individual exit interviews, and c) develop and modify initial therapist training and process rating measures. Products will include a) a manual for integrated CBT for POD to be used in opioid treatment programs and primary care settings with POD patients, b) therapist training materials, and c) process rating instruments.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •at least 18 years of age
  • •currently in Methadone Maintenance Treatment (MMT) at the APT Foundation in New Haven, CT
  • •opioid dependence
  • •experience moderate to severe chronic pain

排除标准

  • •current suicide or homicide risk
  • •are unable to complete the informed consent or surveys because of psychiatric impairment
  • •have cognitive impairment
  • •are unable to read or understand English

研究组 & 干预措施

1

Other

Integrated Cognitive Behavioral Therapy for pain reduction and opioid dependence.

干预措施: Integrated Cognitive Behavioral Therapy (Behavioral)

结局指标

主要结局

Reduced illicit opioid use and pain

时间窗: 12 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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