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Contribution of Hypnosis During a Lumbar Puncture.

Randomized Controlled Study Evaluating The Contribution of a Hypnosis Intervention During a Lumbar Puncture in the Neurology Department.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05092906
Acronym
HYPNOPLUS
Enrollment
74
Registered
2021-10-26
Start date
2021-11-09
Completion date
2024-03-13
Last updated
2024-06-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain

Keywords

lumbar puncture, anxiety

Brief summary

The purpose of this study is to assess the effect of hypnosis, as add on therapy, on patients requiring a lumbar puncture (LP) as part of their medical management.

Detailed description

This study will follow the zelen's methodology randomization. It is an add-on study design. 1. The study will be presented to patients as an assessment of their comfort during the LP. The intervention group is not presented to the patient. 2. Patients are asked to sign the consent of the standard of care group. 3. Randomization into two equally sized groups: * Intervention arm : LP with complementary hypnoanalgesia * Control arm : LP without complementary hypnoanalgesia 4. Patients who have been randomized into the control group, will have LP according to the standard of care. Patients who have been randomized into the hypnoanalgesic group will be informed about the hypnoanalgesia intervention and then asked to sign the consent of the hypnosis group. * if the patient accepts, he will benefit from hypnosis during LP. * if the patient refuses, he will re-join the control group without hypnosis. The physicians performing LP will be the same in both groups. A phone call follow-up is scheduled on day 3 and 7 after intervention.

Interventions

OTHERLP with complementary hypnoanalgesia

The lumbar puncture technique will be identical to that of the group standard of care. Hypnosis will be performed by a health professional trained in this practice, in addition to the standard analgesic management.

OTHERLP with standard of care

The LP will be carried out according to the usual techniques without hypnosis. Standard analgesic treatments will be used (except contraindications): * EMLA (Lidocain+Prilocain) Cream/Patch * Local anesthesia with lidocain chlorhydrate monohydrate 1% injectable * Nitrous oxide

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Required a lumbar puncture for diagnosis * Affiliated with social security system * Patient's written consent

Exclusion criteria

* LP contraindication * History of previous LP * Psychiatric disorder making the realization of a hypnosis irrelevant * Cognitive-behavioural abilities that do not allow the completion of the study * Persons who are protected under the act. Person deprived of liberty by judicial decision * Pregnant or Breastfeeding woman

Design outcomes

Primary

MeasureTime frameDescription
Maximum pain felt during LPImmediately at the end of LP procedureThe maximum pain experienced will be assessed in the immediate post procedure using a Numeric Pain Rating Scale (NPRS). The NPRS is a 10 points scale, ranging from 0 (no pain) to 10 (maximal pain).

Secondary

MeasureTime frameDescription
Ratio of patients with a Numeric Pain Rating Scale (NPRS) score >= 4.Immediately at the end of LP procedureComparison between the two groups of the ratio of patient with a NPRS \>= 4.
Acceptation of hypnosisDay1Number and percentage of subjects randomized and analyzed in the hypnoanalgesia group and who have actually had hypnosis
Comfort felt during LPImmediately at the end of LP procedureThe comfort level felt during the LP procedure will be assessed with a Numeric Rating Scale (NRS). The NRS is a 10 points scale, ranging from 0 (total uncomfort) to 10 (maximal comfort).
Assess pain at Day 3 and Day 7Three days and then seven days after the LP.The pain level will be assess using the NPRS scale by telephonic interview.
Timeframe for resumption of usual activities.Seven days after the LP.Number of days between LP and the resumption of usual activities
State and Trait anxiety before LPBefore randomizationThe state and trait anxiety will be assess using the State and Trait anxiety inventory (STAI) questionnaire.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026