Actively Recruiting
Pain Management With Virtual Reality Hypnosis
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-05-25
142
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The latency phase corresponds to the first phase of the first stage of labour, during which the parturient feels regular, rhythmic uterine contractions that are often painful, with or without changes of the cervix. This phase lasts an average of 8 hours for primiparous women, compared with 5 hours for multiparous women, and can last up to twenty hours in total. Cervical ripening corresponds to the medical induction of regular, painful uterine contractions in order to obtain a favourable cervix for the induction of labour. Cervical ripening is carried out either medically (oral or local prostaglandins) or mechanically (double balloon dilatation) and accounts for 69.2% of labour inductions, which in turn account for 25.8% of births. At Amiens-Picardie University Hospital, this maturation stage can last from a few hours to 2 days, depending on the service protocol. What these two stages of childbirth have in common is that they are both painful, with very few analgesic drugs available that can be used without side-effects on the foetus during pregnancy. In recent years, there has also been a growing demand from parturients for the use of non-medicinal therapies. It therefore seems essential to provide parturients with as many effective non-drug methods as possible to manage their pain properly. If virtual reality hypnosis sessions prove to be effective, they will provide better pain management for women in labour, reduce the use of morphine derivatives (with their attendant side-effects, particularly on the foetus), and above all meet the growing demand from women in labour for the most physiological possible support during childbirth.
CONDITIONS
Official Title
Pain Management With Virtual Reality Hypnosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Woman aged 18 years or older
- Speaks and understands French
- Hospitalized before labor begins
- Membranes intact or ruptured
- Experiencing spontaneous or induced labor
- In the latency phase of labor
- Pregnancy term of at least 37 weeks
- END score greater than 3
- Requires active pain management (medicinal or non-medicinal)
- Low-risk pregnancy
You will not qualify if you...
- Under legal protection
- Hearing impairment
- Visual impairment
- Epilepsy
- Psychiatric problems
- Pathological pregnancy
- Chronic pain
- Addiction-related disorders
- Allergy to paracetamol
- Allergy to phloroglucinol
- Allergy to codeine
- Allergy to nalbuphine
- Allergy to orozamudol
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHU Amiens Picardie
Amiens, France
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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