Skip to content

Does Hypnosis Improve Severe Sleepwalking ?

Does Hypnosis Improve Severe Sleepwalking ?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02648568
Acronym
HYPNOSOM
Enrollment
103
Registered
2016-01-07
Start date
2015-01-31
Completion date
2017-12-31
Last updated
2017-12-08

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

Conditions

Sleepwalking

Keywords

Sleepwalking, sleep terrors, arousal disorders, F513 (CIM-10), F514 (CIM-10)

Brief summary

The aim of the study is to compare the benefit of two cognitive therapies in severe sleepwalking/ sleep terrors: relaxation vs. relaxation plus hypnosis. This is a monocentric, double-blind controlled study. 75 patients (aged more than 15 yo) with severe sleepwalking (defined as at least one epsidoe per week and at least two awakenings in stage N3 on video polysomngraphy) will be included. All patients will have a visit 1 for diagnosis including a medical interview, a video polysomnography, questionnaires on sleepwalking (PADSS and systematized interview), sleep quality (PSQI, MEQ) and sleepiness (Epworth scale) and suggestibility scale. 25 patients will be randomized to the relaxation group, 25 patients to the hypnosis plus relaxation group, while the 25 non-randomized patients will be non-treated controls. Randomized patients will receive the therapy on day 1, and be monitored during the subsequent night. They will have a weekly therapy for 4 additional sessions and be monitored again on Month 1, as well as they will complete the sleep and sleepwalking questionnaires. They will also complete the questionnaire by phone on Month 3. The non-randomized controls will complete the questionnaire on month 1, with no therapeutical intervention between Day 1 and Month 1. The main outcome will be the frequency of sleepwalking episodes, as assessed by the PADSS-B. Secondary outcomes include the changes in other subitems of teh PADSS, of the N3 awakenings in v-PSG between night 1 and Night 2 (short term effect) and Night 1 and Night 28 (long term effect), as well as changes in sleep quality and sleepiness scales. A comparison of spectral EEG, as well as respiration, eye movements, muscle tone and heart rate during rest, hypnosis trance, relaxation and sleepwalking episodes is also scheduled.

Detailed description

Extended description of the protocol, including more technical information (as compared to the Brief Summary) if desired. Do not include the entire protocol; do not duplicate information recorded in other data elements, such as eligibility criteria or outcome measures

Interventions

BEHAVIORALHypnosis plus relaxation

The patient will have 20 min of Jacobson 's type relaxation, with sequential contraction and relaxation of limb muscles followed by an induction of hypnosis based on the preferential channel of each patient and, during trance, recommendation to assimilter the bed room and bed to a safe place

BEHAVIORALRelaxation

The patient will have 20 min of Jacobson 's type relaxation, with sequential contraction and relaxation of limb muscles

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

1. \>15 years old 2. French speaker 3. having signed the Informed consent form 4. Affiliated to National Health Insurance 5. Sleepwalking or sleep terrors (ICSD-3 criteria); 6. At least 2 awakenings from N3 on Night 1 videopolysomnography; 7. At least one episode per week.

Exclusion criteria

1. \< 15 years old 2. Patient under guardian ship 3. Patient unable to understand the protocol 4. Patient unable, from investigator's opinion, to comply to the procedures of the trial, including the ability to practice self-hypnosis.

Design outcomes

Primary

MeasureTime frameDescription
Frequency of sleepwalking episodes as assessed by the PADSS-Bat one month (long term)PADSS-B questionnaire, including the frequency of sleepwalking/sleep terrors episodes as evaluated by the patients, from none(0) to (several par nights (6)

Secondary

MeasureTime frameDescription
Objective measures of sleepwalking :behaviors on videoPSGNight 2 (8 hours) and at one month (long term)scale of behaviors on videopSG
% of sleep stagesNight 2 (8 hours) and at one month (long term)sleep stages (% of total sleep time)
total sleep timeNight 2 (8 hours) and at one month (long term)total sleep time in minute
Other subjective characteristics of sleepwalking/sleep terrorsAt one and at three monthstotal PADSS score
Objective measures of sleepwalking: number of N3 awakeningsNight 2 (8 hours) and at one month (long term)Number of N3 awakenings
sleep efficiencyNight 2 (8 hours) and at one month (long term)ratio between total sleep time and total sleep period
Spectral EEG (power)At night 1 (8 hours)Spectral EEG analysis during hypnotic trance, rest, relaxation and N3 awakenings
Eye movements (number per minute)At night 1 (8 hours)EOG during rest, hypnotic trance, relaxation, and N3 awakenings
Muscle tone (amplitude in microvolt)At night 1 (8 hours)chin EMG during rest, hypnotic trance, relaxation, and N3 awakenings
Respiration (Rate of breathing per minute)At night 1 (8 hours)Respiratory rate and amplitude via impedance belts during rest, hypnotic trance, relaxation, and N3 awakenings
Heart rate (beats per minutes)At night 1 (8 hours)heart rate via ECG during rest, hypnotic trance, relaxation, and N3 awakenings
Frequency of sleepwalking episodes as assessed by the PADSS-Bat three months (very long term)PADSS-B questionnaire, including the frequency of sleepwalking/sleep terrors episodes as evaluated by the patients, from none(0) to (several par nights (6)
REM sleep without atoniaAt night 1 (8 hours)Per % of tonic and phasic enhanced muscle tone during REM sleep

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026