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| ID | Type | Description | Link |
|---|---|---|---|
| 372-SR-25 | Other Grant/Funding Number | American Academy of Sleep Medicine Foundation |
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The purpose of this clinical trial is learn whether a behavioral (non-medication) treatment can reduce nightmares in adults with narcolepsy. All participants will receive the treatment and will complete three assessments. Half of the participants will receive the treatment after the first assessment, and half will receive it after the second assessment. Romantic partners of participants with narcolepsy will also be eligible to enroll in the study. Partners will complete three assessments but will not participate in the treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Treatment | Experimental | The Treatment arm will receive the intervention immediately following the first assessment. |
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| Waitlist | Other | The Waitlist arm will undergo a waiting period following the first assessment and then will receive the treatment after the second assessment. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Imagery Rehearsal Therapy (IRT) | Behavioral | The intervention will consist of 7 therapy sessions (once per week for 7 weeks) which will be delivered via videoconference. During the sessions, participants will learn techniques for managing and changing nightmares. |
| Measure | Description | Time Frame |
|---|---|---|
| Disturbing Dream and Nightmare Severity Index (DDNSI) | The DDNSI is a questionnaire which measures the severity of nightmares. | Completed at each of the three assessments (baseline, 10 weeks, 19 weeks) |
| Nightmare frequency (sleep diary) | The number of nightmares experienced each day will be collected on daily sleep diaries completed during each assessment period. | Completed at each of the three assessments (baseline, 10 weeks, 19 weeks) |
| Measure | Description | Time Frame |
|---|---|---|
| PROMIS Anxiety | Questionnaire which measures the severity of anxiety symptoms. | Completed at each of the three assessments (baseline, 10 weeks, 19 weeks) |
| PROMIS Depression | Questionnaire which measures the severity of depressive symptoms. |
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PARTICIPANTS WITH NARCOLEPSY/NIGHTMARES
Inclusion Criteria:
Exclusion Criteria:
PARTICIPANTS WHO ARE PARTNERS OF SOMEONE WITH NARCOLEPSY
Inclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jennifer Mundt, PhD | Contact | 801-646-8287 | DAWNstudy@utah.edu |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Utah | Salt Lake City | Utah | 84108 | United States |
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| ID | Term |
|---|---|
| D009290 | Narcolepsy |
| ID | Term |
|---|---|
| D006970 | Disorders of Excessive Somnolence |
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
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| ID | Term |
|---|---|
| D015928 | Cognitive Behavioral Therapy |
| ID | Term |
|---|---|
| D001521 | Behavior Therapy |
| D011613 | Psychotherapy |
| D004191 | Behavioral Disciplines and Activities |
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Waitlist control
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| Completed at each of the three assessments (baseline, 10 weeks, 19 weeks) |
| D009422 | Nervous System Diseases |
| D001523 | Mental Disorders |