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Testing the Nocturnal Sleep Latency Profile in Primary Insomnia

Testing the Nocturnal Sleep Latency Profile in Primary Insomnia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00167375
Enrollment
24
Registered
2005-09-14
Start date
2005-01-31
Completion date
2007-06-30
Last updated
2008-02-15

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

Conditions

Primary Insomnia, Sleep Initiation and Maintenance Disorders

Keywords

Insomnia, polysomnography, sleep onset, time series analysis

Brief summary

This study tests a new kind of sleep study in which subjects are awakened 2 times after initially going to sleep. The study focuses on the EEG signal process as a person goes to sleep. The general hypothesis is that the signal properties are stable from night to night during baseline studies, and are different between controls and patients with primary insomnia. The primary insomnia patients then go on to have about 2 weeks of an insomnia intervention. Then the new kind of study is repeated in the patients. The controls only are examined in baseline studies.

Detailed description

Patients are carefully screened to have DSM primary insomnia, and do not have another disorder than may cause a sleep disturbance. After a 2-week baseline period, the subjects undergo a screening sleep study to rule out sleep apnea and periodic limb movement disorder. Then they undergo the NSLP procedure. In that procedure, there pre-bedtime EEG recordings and questionnaire responses taken. Then at a planned time, the subjects go to bed and try to sleep while there EEG signals are recorded. After the first and second sleep cycles, they are awakened for one minute, then asked to return to sleep. In the morning additional recordings and questionnaire responses are obtained. Two nights later they repeat a baseline NSLP procedure. The controls then end their participation. The Patients then receive an open treatment with eszopiclone and behavioral treatments so that their insomnia may improve. After 2 weeks intervention, the patients complete one NLSP night. The goal of the study is to see if there can be data to support the idea that the sleep onset process might harbor a sign of primary insomnia that could be used for the development of a better medical model of primary insomnia.

Interventions

BEHAVIORALGeneral cognitive/behavioral interventions for insomnia

Sponsors

American Academy of Sleep Medicine
CollaboratorOTHER
Sumitomo Pharma America, Inc.
CollaboratorINDUSTRY
University of Pittsburgh
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Primary Insomnia (N = 12) Age & Gender matched Healthy controls (N = 12)

Exclusion criteria

* Unstable Medical illness No other Sleep disorder BMI \> 35, AHI \> 10, PLM Index \> 10, Ferritin \< 50. Unable to communicate in English

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026