Combined Treatment of Nightmares With Targeted Memory Reactivation and Imagery Rehearsal Therapy
- Conditions
- Nightmares, REM-Sleep Type
- Interventions
- Behavioral: Imagery Rehearsal Therapy and Targeted memory reactivation during REM sleepBehavioral: Imagery Rehearsal Therapy
- Registration Number
- NCT05237778
- Lead Sponsor
- University Hospital, Geneva
- Brief Summary
With this protocol, investigators examine whether targeted memory reactivation (TMR), a technique used to strengthen memories, can accelerate remission of nightmare disorder. This protocol uses TMR during REM sleep to strengthen positive memories generated by Imagery Rehearsal Therapy (IRT), a recommended treatment of nightmares. Patients with nightmare disorder are asked to perform an initial IRT session and, while they generate a positive outcome of their recurrent nightmare, half of the patients are exposed to a sound (TMR group), while no such pairing with a sound takes place for the other half (control group). During the next two weeks, all patients perform IRT every evening at home and are exposed to the sound during REM sleep with a wireless headband, which automatically detects sleep stages. Clinical evaluation of the severity of nightmares before and after (2-weeks follow-up and 3-months follow-up) this intervention takes place using the validated Nightmare Frequency Questionnaire (NFQ, primary outcome measure), which retrospectively identifies the frequency of nightmares. We hypothesize that patients treated with IRT and who are exposed, during REM sleep and over 14 nights, to a sound that had previously been associated with the new positive dream scenario of IRT (TMR group), will have more reduced frequency of nightmares compared to participants with stimulation of the same, but non-associated, sound during REM sleep (control group).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 36
- Diagnosis of nightmare disorder according to the International Classification of Sleep Disorders (ICSD-3) diagnostic and coding manual
- Patients with at least moderate severity (>1 episode per week)
- severe depression
- insomnia disorder
- psychosis or anxiety disorder
- other sleep disorder (e.g.,obstructive sleep apnea syndrome, restless legs syndrome)
- neurological disease
- use of medications that would be likely to produce nightmares (e.g. hypnotics, β-blockers, amphetamines, antimicrobial agents)
- use of anxiolytics, antipsychotic or antidepressant medication were excluded.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TMR group Imagery Rehearsal Therapy and Targeted memory reactivation during REM sleep Patients will receive a sound while they generate a positive outcome of imagery rehearsal therapy (IRT). They will also receive the sound during REM sleep. Control group Imagery Rehearsal Therapy Patients will not receive a sound while they generate a positive outcome of imagery rehearsal therapy (IRT). They will receive the same sound as the experimental group during REM sleep under the same conditions.
- Primary Outcome Measures
Name Time Method Nightmare Frequency Questionnaire (NFQ) 3 months Validated self-report scale to assess the number of nightmares per week
- Secondary Outcome Measures
Name Time Method Beck Depression Inventory (BDI-II) 3 months Validated self-report scale to assess depressive symptoms
Nightmare Distress Questionnaire (NDQ) 3 months Validated self-report scale to assess the emotional disturbance attributed to the nightmares
Pittsburgh Sleep Quality Index (PSQI) 3 months Validated self-report scale to assess the quality of sleep
Proportion of the emotion 'fear' in dreams 2 weeks Use of a dream diary
Proportion of the emotion 'joy' in dreams 2 weeks Use of a dream diary
Trial Locations
- Locations (1)
Center for Sleep Medicine, University Hospitals of Geneva
🇨🇭Geneva, Switzerland