Combined Treatment of Nightmares With Targeted Memory Reactivation and Imagery Rehearsal Therapy

University Hospitals (UH)

Status: Completed

Conditions: Nightmares, REM-Sleep Type

Treatments: Behavioral: Imagery Rehearsal Therapy and Targeted memory reactivation during REM sleep; Behavioral: Imagery Rehearsal Therapy

Study type: Interventional

Funder types: Other

Identifiers

NCT05237778

2019-02270

Details and patient eligibility

About

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).

Enrollment: 36 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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)

Exclusion criteria

• 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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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36 participants in 2 patient groups

TMR group

Experimental group

Description:

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.

Treatment:

Behavioral: Imagery Rehearsal Therapy and Targeted memory reactivation during REM sleep

Control group

Active Comparator group

Description:

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.

Treatment:

Behavioral: Imagery Rehearsal Therapy