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Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery. (Hypnoanxiety)

H

HASSAN 1st university

Status

Enrolling

Conditions

Postoperative Pain
Length of Stay
Abdominal Surgeries
Hypnosis
Preoperative Anxiety

Treatments

Other: Clincal hypnosis

Study type

Interventional

Funder types

Other

Identifiers

NCT07370974
Hypnosis UHP

Details and patient eligibility

About

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.

Enrollment

48 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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 mental illness
    4. Psychoactive substance consumption
    5. Cognitive disorders

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

48 participants in 2 patient groups

Fisrt arm: patients having a session of hypnosis prior to surgery
Experimental group
Description:
Patients randomized to the intervention arm undergo a single 15-20 minute clinical hypnosis session preoperatively for anxiety reduction, achieving level 2 hypnotic trance (somnambulism)
Treatment:
Other: Clincal hypnosis
Arm 2 : patients will be treated as usual with standard conditions
No Intervention group
Description:
Patients in this group will receive standard usual care without any hypnotic intervention, only with routine psychological preparation.

Trial contacts and locations

3

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Central trial contact

YOUSSEF EL-ALLAM EL-ALLAM, Phd student; NAOUFAL HIMMOUCHE Pr Himmouche, Professor

Data sourced from clinicaltrials.gov

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