BEnefit of HYpnosis on Pain during stitches in an Emergency Room: a study protocol using a randomised controlled trial - the BE-HYPER protocol.
Léa Pérard, Maëlys Clinchamps, Frédéric Dutheil...
https://pubmed.ncbi.nlm.nih.gov/42425558/Actively Recruiting
Led by University Hospital, Clermont-Ferrand · Updated on 2026-06-02
180
Participants Needed
1
Research Sites
N/A
Total Duration
This research aims to evaluate the impact of hypnosis on pain and stress during stitches in patients with skin wounds treated in an emergency department. The study focuses on measuring heart rate variability as a way to assess stress response during the procedure. It is a randomized, controlled, single-center, prospective study involving adults admitted to the emergency department with stitchable wounds. Participants will be randomly assigned to one of two groups one group will receive hypnosis performed by a trained person before stitching, and the other will receive the standard care without hypnosis. All patients will wear a heart rate monitoring belt, and both groups will undergo stitching as usual. Blood samples, heart rate, and blood pressure will be measured before and 30 minutes after the procedure, along with self-assessment questionnaires on pain and stress. During the study, participants will complete pain and stress questionnaires before and after stitching, and a blood sample will be collected twice to evaluate stress biomarkers. Heart rate and blood pressure will be monitored continuously. After the final assessment, the heart rate monitoring belt will be removed, and the study will conclude for the patient. The main outcome is heart rate variability at the time of stitching, with additional evaluations of pain, stress, and physiological markers over the brief study period.
CONDITIONS
BEnefit of HYpnosis on Pain During Stitches in Emergency Room
L
LISE LACLAUTRE
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
University Hospital, Clermont-Ferrand
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - Up to 1 day
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Approximately 30 minutes
Participants receive either hypnosis before stitches or standard care without hypnosis while undergoing stitching in the emergency room.
1 treatment visit (in-person)
Duration - 30 minutes after treatment
Participants complete pain and stress self-assessment questionnaires and provide a blood sample after the stitching procedure.
1 follow-up assessment (in-person)
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
Have more questions? Get in touch with our team for quick support
Léa Pérard, Maëlys Clinchamps, Frédéric Dutheil...
https://pubmed.ncbi.nlm.nih.gov/42425558/University Hospital, Clermont-Ferrand
Lead Sponsor