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临床试验/NCT06499909
NCT06499909已完成不适用

Hypnosis for the Management of Postoperative Pain Following Colectomies: a Single Centre Randomised Controlled Feasibility Trial

Somerset NHS Foundation Trust2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2023年6月6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
42
试验地点
2
主要终点
The effectiveness of hypnotic analgesia on post-operative pain after colectomies.

研究概览

简要总结

The present study intends to assess the feasibility, value and direction of conducting a future, full scale randomised controlled trial, to evaluate the effects of clinical hypnosis on post-operative pain, following colectomy operations.

Pain management in the postoperative setting presents a challenge as the development and severity of pain after surgery is dependent on different patient and procedural factors. Furthermore, pain after surgery is a major concern for patients, especially when it is undermanaged. When postoperative pain control is suboptimal it delays mobilisation, reduces oral food and fluid intake after surgery, and increases the risk of developing chronic pain and other complications. These factors have a negative impact on the patient recovery process, thus increasing the length of hospital stay and healthcare costs. Hypnosis is well recognised as having an effect in pain perception, it is a brief, easy to administer intervention making it a promising non-pharmacological intervention with the potential to help postoperative pain management in patients undergoing colectomies as well as reducing anxiety and emotional stress related to surgery, while also having a positive indirect effect on recovery times, which could lead to considerable cost-savings at organisational level.

The intervention will be delivered at Somerset NHS Foundation Trust by a designated Principal Investigator. Hypnosis sessions will be given face to face in a clinical consulting room and on the ward where the participants will be admitted after surgery. The study aims to enrol 40 participants, 20 for each arm, over 12 months, from Musgrove Park Hospital who will undergo elective colectomy surgery. Eligible participants would be adults 18 years or over, undergoing elective colectomy surgery. Participants must be able to provide a written informed consent and able to understand and communicate in English.

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
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

入选标准

  • Patients will be included in the study if they meet ALL of the following inclusion criteria
  • Aged 18 years or over;
  • Undergoing elective colectomy surgery (open and laparoscopic colectomies will be included).
  • Patients that can provide written informed consent.
  • Are able to understand and communicate in English.

排除标准

  • A patient meeting ANY of the following exclusion criteria at baseline will be excluded from participation:
  • Emergency colectomies will be excluded due to the urgency of the intervention.
  • Non English speakers.
  • Patients with the following diagnosed mental health illness: personality disorders, psychosis or schizophrenia as hypnosis could aggravate these conditions.
  • Patients that are already involved in other research studies and that could influence the results of the study.
  • Any patient that is clinically unwell post-surgery with a National Early Warning Score (NEWS) of 5 or higher. NEWSscore is a tool developed for NHS England which improves the detection and response to clinical deterioration in adult patients and is a key element of patient safety and improving patient outcomes.
  • Patients with deafness or difficulty hearing as this would be essential for this therapy to be effective.

研究组 & 干预措施

Hypnosis

Experimental

Patient receives hypnosis treatment prior to surgery

干预措施: Hypnosis (Other)

Normal care pathway

No Intervention

Patient will receive standard care

结局指标

主要结局

The effectiveness of hypnotic analgesia on post-operative pain after colectomies.

时间窗: 365 days

The investigator is assessing the effectiveness of hypnosis on pain by using numeric pain scales to assess pain scores before and after hypnosis. This will then help the investigator evaluate pain scores between groups and compare the before and after hypnosis scores.

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 (2)

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