The Psychoneuroimmunology of Insomnia

NCT ID: NCT00680771

Last Updated: 2012-10-17

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 28 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2008-03-31
• Study Completion Date: 2010-07-31

Brief Summary

Chronic insomnia affects approximately 8-9% of the population. The prevalence of this disorder rises dramatically across the lifespan, especially so in women. When it is chronic, insomnia is associated with increased fatigue, cognitive impairment, mood disturbance, physical complaints, diminished quality of life and increased health care consumption. There is also more limited evidence (based on epidemiologic studies or experimental studies in healthy subjects) that insomnia and/or sleep loss may be a risk factor for hypertension and/or cardiovascular disease and increased mortality.

Despite its prevalence and consequences, the pathophysiology of insomnia and, specifically, the pathway by which morbidity risk is conferred, has been relatively unstudied. With respect to medical illness in particular, insomnia may confer risk in several ways, including: 1) an inherent compromise in the restorative/conservative function of sleep, 2) the deleterious effects of "hyperarousal" and/or HPA axis abnormalities on end organ integrity and function, and/or 3) diminished immunocompetence. This study focuses on the last of these possibilities, the relationship between immune function and sleep.

The study compares immune response to a vaccine challenge in two groups: good sleepers and patients with chronic insomnia. The primary study hypothesis is that the insomnia group will have a decreased rate of adaptive immune response to the vaccine challenge than that of the good sleeper group.

Conditions

Primary Insomnia

Keywords

Primary Insomnia; Insomnia; Good Sleepers; Hep B; Vaccine

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

1

Primary Insomnia

No interventions assigned to this group

2

Good Sleepers

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

Their sleep schedule will include a typical bedtime of between 9:00 p.m. and 12:00 a.m. to minimize circadian rhythm influences on the diagnoses of Primary Insomnia (PI).

PIs will also meet the sleep disturbance criteria of the Pittsburgh Sleep Quality Index(PSQI) > 5 and the Insomnia Severity Index (ISI)> 15 and one of the following minimal characteristics both at intake and as an average profile from the two weeks of baseline diaries: > 30 min. sleep-onset latency (SL), > 30 min. of wake after sleep-onset (WASO), Early Morning Awakening >30 min. prior to the desired wake up time, or any two of the above complaints (Mixed Insomnia); Total Sleep Time (TST) < 6 hours [unless the Sleep Efficiency is < 80%] and the problem frequency must be > 3 nights/week; problem duration > 6 months.

Good Sleeper participants will report that they obtain enough sleep and that their sleep is restorative with average SL and WASO < 15 minutes, TST > 6 hours ESS < 5 on the ESS, < 5 on the PSQI, and < 7 on the ISI.

Exclusion Criteria

• any conditions contraindicated by the vaccine manufacturer or any history of allergic reactions to vaccines
• Undergoing and/or taking immunosuppressive therapies
• Sero-positive for Hep B antibodies
• Inadequate language comprehension
• Menopause, peri-menopause or premenstrual syndrome
• Pregnancy
• Unstable medical or psychiatric illness
• History of head injury with a sustained loss of consciousness
• Evidence of active illicit substance use or fitting criteria for alcohol abuse or dependence
• Use of medications thought to alter sleep such as stimulants, sedating antidepressants, and hypnotics
• Symptoms suggestive of sleep disorders other than Insomnia
• Polysomnographic data indicating sleep disorders other than Insomnia

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute of Nursing Research (NINR)

NIH

Sponsor Role: collaborator

University of Rochester

OTHER

Sponsor Role: lead

Responsible Party

Wilfred Pigeon

Assistant Professor of Psychiatry

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Wilfred R Pigeon, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of Rochester

Locations

University of Rochester Sleep Research Laboratory

Rochester, New York, United States

Countries

United States

Other Identifiers

1K23NR010408

Identifier Type: NIH

Identifier Source: secondary_id

View Link

RSRB # 19132

Identifier Type: -

Identifier Source: org_study_id