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临床试验/NCT05098158
NCT05098158已完成不适用

Community-Engaged Options to Maximize and Facilitate Opioid Reduction Through Treatment

Washington State University2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2020年7月10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
21
试验地点
2
主要终点
Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity Rating

研究概览

简要总结

This study investigates how adults prescribed opioids for chronic noncancer pain respond to invitations to try non-opioid options of massage therapy, yoga therapy, chiropractic and physical therapies. Options will be available via telehealth consultation visits using a computer or smartphone with internet connection. The investigators will measure effects on pain, pain-related symptoms, and opioid use over time using a single-group design.

详细描述

Participants will be recruited from local primary care practices and asked to complete a baseline survey. They will then meet with a registered nurse via teleconference for a complete pain assessment. At the end of the session, participants will be asked to choose two of four available modalities for telehealth consultation. Participants will be scheduled for six telehealth sessions, once per week x six weeks with three consultations per each chosen therapy. Measurements of pain, mood, sleep, medicine use will be captured at baseline, three weeks and six weeks and examined for changes over time.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

  • •enrollment in treatment at the CHAS Perry St or partnering clinic;
  • •age greater than 18 years;
  • •ability to read, speak, and write English;
  • •diagnosed with a chronic, non-cancer-based painful medical condition;
  • •ability to provide informed consent.

排除标准

  • •pregnancy;
  • •diagnosis of a cancer-based painful medical condition;
  • •any other medical or psychiatric condition that the PI or Co-PI physician of record determine might compromise safe study participation (including but not limited to active psychosis, history of frequent psychiatric hospitalizations, severe anxiety with claustrophobia, aggression)

研究组 & 干预措施

Single arm pain treatment

Experimental

Arm includes usual pain care plus the chosen two telehealth interventions x 6 weeks

干预措施: Non-pharmacological pain treatment (Other)

结局指标

主要结局

Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity Rating

时间窗: 6 weeks

Full scale name is PROMIS (Patient-Reported Outcome Measurement Information System) Pain Intensity Scale version 3a that measures the construct pain intensity or severity in three items for how much it hurts on average, at its worst and at its least in the past 7 days. Scale ranges from minimum "no pain" =1 to maximum "very severe" =5 pain with a possible sum of 3-15. A total sum of the 3 items is converted into a T-score where 50 is equivalent to the U.S. general population average and + /- 10 points is equivalent to the standard deviation. Higher values are considered to be a worse outcome (range 40-70 after T-score conversion).

PROMIS Pain Interference Rating

时间窗: 6 weeks

Scale name is PROMIS (Patient-Reported Outcome Measurement Information System) Pain Interference Scale that measures the construct pain interference in 8 items for how much pain interferes with a variety of activities in the past 7 days. Scale ranges from minimum "not at all" =1 to maximum "very much" =5 pain with a possible sum of 8-40. A total sum of the 8 items is converted into a T-score where 50 is equivalent to the U.S. general population average and + /- 10 points is equivalent to the standard deviation. Higher values are considered to be a worse outcome.

次要结局

  • Current Opioid Misuse Measure(6 weeks)
  • Spiritual Well-being Index(6 weeks)
  • Interpersonal Needs Questionnaire(6 weeks)
  • Depressive Symptoms Using Patient Health Questionnaire (PHQ-8)(6 weeks)
  • PROMIS Self-efficacy for Managing Symptoms Short Form 4a(6 weeks)
  • PROMIS Self-efficacy for Managing Emotions Short Form 4a(6 weeks)
  • Anxiety Using Generalized Anxiety Disorder (GAD-7)(6 weeks)
  • Interpersonal Needs Questionnaire(6 weeks)
  • Current Opioid Misuse Measure(6 weeks)
  • Spiritual Well-being Index(6 weeks)

研究者

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

Marian Wilson

Associate Professor

Washington State University

研究点 (2)

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