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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04368572
Other study ID # 2019-A00447-50
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date June 2020

Study information

Verified date April 2020
Source Gérond'if
Contact Anaïs Cloppet-Fontaine, MD
Phone +33 (0) 185781010
Email anais.cloppet@gerondif.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Lumbar puncture is a diagnostic procedure performed as part of the etiological assessment of cognitive disorders. Despite good tolerance and very rare complications, lumbar puncture is still perceived as being painful or anxiety-provoking by patients. Hypnosis could improve pain and anxiety when performing lumbar puncture.


Description:

Lumbar puncture is an invasive procedure potentially inducing pain and anxiety indicated in elderly patients for cognitive assessment. Indeed, the measure of amyloid biomarkers and tau in the cerebrospinal fluid is useful in the etiological diagnosis of cognitive disorders. With the ageing of the population and the increase incidence of cognitive disorders, this diagnostic procedure will be more and more frequent. Many studies have shown the efficiency of hypnosis during invasive procedure, especially in young children. The absence of side-effect is a major asset in elderly patients at high iatrogenic risk. It represents an interesting alternative to anxiolytic or sedative treatments. Nevertheless, its effectiveness in the elderly during lumbar puncture remains to be demonstrated. Investigators hypothesized that hypnosis may decrease pain and anxiety during lumbar puncture associated to setting comfort situation (relational care, music, transcutaneous anesthesia).


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 2020
Est. primary completion date May 2020
Accepts healthy volunteers No
Gender All
Age group 70 Years and older
Eligibility Inclusion Criteria:

- Age = 70 years old

- Indication for a lumbar puncture for etiological diagnosis of cognitive impairment

- Understanding French Language

- Written and informed consent for this study signed by the patient

- Affiliated to Health Insurance

Exclusion Criteria:

- MMS< 17 or cognitive impairment not allowing informed consent

- Contraindication to lumbar puncture

- Refusal to sign the written and informed consent

- Patient deprived of freedom by court or administrative order

Study Design


Intervention

Behavioral:
Hypnosis
An interview assesses the patient's level of anxiety, interests and dissociative abilities. Hypnosis is done by following the steps: First step: reception and installation of the patient Second step: induction phase Third step: hypnotic trance phase Fourth step: reorientation phase

Locations

Country Name City State
France Geriatric Department, Bichat hospital Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Gérond'if

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-reported pain during the lumbar puncture Pain is assessed by visual analogue scale, a self-reported pain rating scale (0 "no pain" to 10 "worst pain") 1 day
Secondary Pain assessed by the physician during the lumbar puncture using Algoplus© score Algoplus© score is an acute pain-behaviour scale for older people with inability to communicate verbally (0 "No pain" to 30 "worst pain") 1 day
Secondary Assessment of anxiety during the lumbar puncture according a visual analogue scale Anxiety is evaluated by the patient with a visual analogue scale (0 "No anxiety" to 10 "Worst anxiety) 1 day
Secondary Assessment of anxiety during the lumbar puncture according a numeric scale Anxiety is evaluated by the physician with a numeric scale (0 "No anxiety" to 10 "Worst anxiety) 1 day
Secondary Assessment of anxiety during the lumbar puncture by monitoring the heart rate 1 day
Secondary Assessment of anxiety during the lumbar punctureby monitoring the Galvanic Skin Response 1 day
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