Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06502457

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Trial Site Locations

Total: 1 location

1

CHU Amiens Picardie

Amiens, France

Actively Recruiting

Loading map...

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

Not the Right Trial for You?

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