ISRCTN57050216已完成未知
Multiple Symptoms Study 3: pragmatic trial of a community based clinic for patients with persistent (medically unexplained) physical symptoms
HS Sheffield Clinical Commissioning Group0 个研究点目标入组 354 人开始时间: 2018年10月2日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 354
研究概览
简要总结
2022 Protocol article in https://pubmed.ncbi.nlm.nih.gov/36379663/ (added 23/11/2022) 2024 Results article in https://doi.org/10.1016/s0140-6736(24)00700-1 (added 17/06/2024)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Aged between 18 – 69 years (inclusive) at the time of the computer search
- •2. Current physical symptoms which meet the below criteria:
- •2.1. Clinical records suggest MUS (presence of at least one code for an MUS syndrome or at least two codes for negative investigations)
- •2.2. Records show at least 2 referrals for specialist opinion or diagnostic investigations in the last 3 years
- •2.3. Records show no evidence of any previous or current major illnesses likely to cause multiple symptoms
- •2.4. Doctors in the GP practice do not believe that the majority of the patient’s symptoms can be currently explained by other pathology
- •2.5. The score on the self-completed PHQ-15 symptoms scale is between 10 and 20 (inclusive)
- •SUB-STUDY - Pen and brief PIS
- •Any patient identified in the GP mail out as eligible to receive an MSS3 trial invitation pack will be entered into the pen and brief PIS sub-study
排除标准
- •1. A score of 3 on question 9 relating to thoughts of self-harm on the PHQ-9 completed at the baseline visit*
- •2. Difficulty conducting a healthcare consultation in English without either a professional or family interpreter or other assistance (either indicated in GP records, or becoming apparent during the enrolment and consent process)
- •3. The GP regards inviting them to participate as inappropriate (e.g. recent bereavement)
- •4. Severe symptom-related disability (e.g. requiring help with daily personal care or severely impaired mobility)
- •5. Undergoing active multidisciplinary rehabilitation, IAPT programme or specialist psychological treatment including specialist pain, fatigue or other symptom clinic at the time of screening.
- •6. Currently pregnant** or less than 6 months postnatal at the time of the screening telephone call
- •*If a score of 3 is identified at any time point during the study the suicide protocol will be triggered
- •**if a participant becomes pregnant after the screening telephone call they will remain in the study and continue to attend the Symptoms Clinic Intervention if allocated to the intervention group.
- •SUB-STUDY - Pen and brief PIS
- •There are no additional exclusion criteria for the pen and brief PIS sub-study
研究者
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