Hypnosis for Reducing Anxiety in Abdominal Surgery
Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery.
Recruiting
N/AInterventional Study
HypnosisPreoperative AnxietyPostoperative PainAbdominal SurgeriesLength of Stay
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
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At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
48 (estimated)
Sponsor
HASSAN 1st university · Other
Who this trial is looking for
This trial is looking for adults who are having abdominal surgery and want to try hypnosis to reduce anxiety before the operation. Participants will either receive hypnosis or standard preparation to help them feel less anxious.
Are You a Good Fit for This Trial?
You may be able to join if
I am an adult.
I have agreed to participate.
I am having abdominal surgery.
I am in ASA physical status I or II.
I can understand and follow instructions.
You may not be able to join if
I do not want to participate.
I have used hypnosis before.
I have a history of mental illness.
I consume psychoactive substances.
I have cognitive disorders.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This Multicenter randomized controlled trial evaluates clinical hypnosis efficacy for reducing perioperative anxiety and postoperative pain in abdominal surgery patients across 3 Moroccan centers (n=48-68). Intervention arm receives 15-20 min level 2 hypnosis session preoperatively; control receives standard psychological preparation. Primary outcome: VAS-anxiety post-intervention. Secondary: post…
This Multicenter randomized controlled trial evaluates clinical hypnosis efficacy for reducing perioperative anxiety and postoperative pain in abdominal surgery patients across 3 Moroccan centers (n=48-68). Intervention arm receives 15-20 min level 2 hypnosis session preoperatively; control receives standard psychological preparation. Primary outcome: VAS-anxiety post-intervention. Secondary: postoperative EVA-pain, analgesic consumption, length of stay.
Study Design Prospective, multicenter, parallel-group RCT (1:1 allocation, stratified by center/sex). Inclusion: consenting ASA I-II adults for abdominal surgery. Primary endpoint powered for 10mm EVA reduction (80% power, α=0.05). Registration supports PhD thesis at ISSS/Université Hassan 1er Settat.
Trial Locations
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Eligibility Criteria
* Inclusion Criteria:
1. Consenting patients undergoing abdominal surgery
2. ASA I-II physical status
3. Able to understand and respond to instructions
4. No major psychological disorders
* Exclusion Criteria:
1. Non-consenting patients
2. Prior experience with hypnosis
3. History of…
* Inclusion Criteria:
1. Consenting patients undergoing abdominal surgery
2. ASA I-II physical status
3. Able to understand and respond to instructions
4. No major psychological disorders
* Exclusion Criteria:
1. Non-consenting patients
2. Prior experience with hypnosis
3. History of mental illness
4. Psychoactive substance consumption
5. Cognitive disorders
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