Insomnia Clinical Trial
— NAPOfficial title:
Non-deceptive Application of Placebos in Insomnia
Verified date | April 2021 |
Source | Philipps University Marburg Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate whether non-deceptive application of a placebo has an impact on subjective or objective sleep parameters in patients with primary insomnia.
Status | Completed |
Enrollment | 51 |
Est. completion date | January 31, 2020 |
Est. primary completion date | January 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 69 Years |
Eligibility | Inclusion Criteria: - age between 18 years to 69 years - fluent in German language - provide written informed consent - ability to understand the explanations and instructions given by the study physician and the investigator Exclusion Criteria: - evidence for sleep disorders caused by medical factors (e.g. sleep apnea, restless legs syndrome, narcolepsy, substance-induced insomnia) - allergies to ingredients of placebo - patients scoring below 8 or above 21 on the Insomnia Severity Index - patients suffering from a mental disorder as verified by the SCID - patients suffering from an acute physical illness - nicotine consumption > 10 cigarettes/day - unwillingness to refrain from alcohol consumption throughout the study - change in concomitant medication regime during the last 2 weeks prior to visit 1 or after randomization - intake of psychotropic drugs during the last 3 months prior to visit 1 - currently pregnant (verified by urine pregnancy test) or lactating |
Country | Name | City | State |
---|---|---|---|
Germany | Department of Clinical Psychology and Psychotherapy, Philipps-University Marburg | Marburg |
Lead Sponsor | Collaborator |
---|---|
Philipps University Marburg Medical Center |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Self-reported Total Sleep Time | assessed by sleep diary | change from baseline to 1 night after placebo intake | |
Secondary | Objective Sleep Efficiency | assessed by actigraphy | change from baseline to 1 night after placebo intake | |
Secondary | Objective Total Sleep Time | assessed by actigraphy | change from baseline to 1 night after placebo intake | |
Secondary | Objective Total Sleep Time | assessed by polysomnography | change from baseline to 1 night after placebo intake | |
Secondary | Objective Sleep Onset Latency | assessed by polysomnography | change from baseline to 1 night after placebo intake | |
Secondary | Self-reported Sleep Onset Latency | assessed by sleep diary | change from baseline to 1 night after placebo intake |
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