An interventional study of Sleep Deprivation in Healthy, sponsored by University of Colorado, Denver. Completed at 1 site in United States. Open to male participants aged 20 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-07-12.
Sponsored by University of Colorado, Denver · Not applicable, Interventional, and Other
This is a small intervention study with healthy males aged 20-65 years old who habitually sleep 7-9 hours/night.This study investigates if and how sleep restriction, independent of circadian misalignment (e.g. shift work, jet lag), induces a decrease in the bone formation marker Procollagen I Intact N-Terminal Propeptide (PINP). The specific aim is to evaluate the mechanistic underpinnings for the relationship between sleep restriction and suppression of bone formation. The study will enroll 12 healthy male participants and have a two-week intervention after enrollment.
University of Colorado, Denver is the lead sponsor of 1,499 studies on the registry; 315 are open to participants now.
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o Adult men aged 20-65 years old who habitually sleep 7-9 hours/night.
Exclusion Criteria:
Self-reported or newly diagnosed medical condition that is still being investigated or is not under good control, including those identified on screening labs such as:
Any clinically significant psychiatric condition, as defined by DSM-V. Individuals with a history of most psychiatric illnesses or psychiatric disorders will be excluded, such as but not limited to depression, anxiety, alcoholism, drug dependency, schizophrenic disorders, and personality disorders (performed by medical history and physician interview). However, a personal history of limited prior counseling, psychotherapy (e.g., for adjustment reactions) will NOT be exclusionary. Evaluation of Psychiatric/Psychological Suitability:
Behavioral: Sleep Deprivation
Participants in this arm will sleep for 8 hours at their habitual time for 1 week outpatient. Food will be provided for the outpatient week by the study. After the outpatient week participants will check into our inpatient Clinical Translational Research Center (CTRC) for a 9 day inpatient stay. During their inpatient stay participants will be sleep restricted to a 5 hour/night sleep opportunity for nights 2-7 of their inpatient stay. Outcome measures include a 24-hour serum draw (urine and blood) which will occur on night 1 (pre) and night 8 (post). Patients will be given a 10 + hour recovery sleep period on night 8 of their inpatient stay.
Change in Serum Pro-collagen 1 Intact N-terminal Propeptide (P1NP)
A marker of bone formation
Time frame: 24 hour serum draw before and after 6 night sleep restriction. Pre measures taken on night 1 through day 2. Post measures taken on night 7 through day 8. A fasting blood sample will be taken each morning of the inpatient stay.
Change in Serum C-telopeptide of Type 1 Collagen (CTX)
A marker of bone resorption
Time frame: 24 hour serum draw before and after 6 night sleep restriction. Pre measures taken on night 1 through day 2. Post measures taken on night 7 through day 8. A fasting blood sample will be taken each morning of the inpatient stay.
| Milestone | Sleep Deprivation |
|---|---|
| Started | 12 |
| Completed | 12 |
| Not completed | 0 |
A marker of bone formation
| ng/mL | Sleep Deprivation |
|---|---|
| Baseline | 72.1 ± 4.4 |
| Sleep Restricted | 67.4 ± 4.4 |
A marker of bone resorption
| ng/mL | Sleep Deprivation |
|---|---|
| Baseline | 0.197 ± 0.05 |
| Sleep Restricted | 0.459 ± 0.06 |
Collected over Adverse events data were collected while subjects were enrolled in the study. This included during their screening visit and during the 16 -37 days they were enrolled in the study.. Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Sleep Deprivation | 0/12 (0%) | 0/12 (0%) | 2/12 (16.7%) |
| Event | Sleep Deprivation |
|---|---|
| Dry eyesEye disorders | 1/12 |
| IrritationSkin and subcutaneous tissue disorders | 1/12 |
| Age, Categorical(Participants) | Sleep Deprivation |
|---|---|
| <=18 years | 0 |
| Between 18 and 65 years | 12 |
| >=65 years | 0 |
| Age, Continuous(years) | Sleep Deprivation |
|---|---|
| Mean | 28.3 ± 5.7 |
| Sex: Female, Male(Participants) | Sleep Deprivation |
|---|---|
| Female | 0 |
| Male | 12 |
| Ethnicity (NIH/OMB)(Participants) | Sleep Deprivation |
|---|---|
| Hispanic or Latino | 0 |
| Not Hispanic or Latino | 12 |
| Unknown or Not Reported | 0 |
| Race (NIH/OMB)(Participants) | Sleep Deprivation |
|---|---|
| American Indian or Alaska Native | 0 |
| Asian | 4 |
| Native Hawaiian or Other Pacific Islander | 0 |
| Black or African American | 2 |
| White | 6 |
| More than one race | 0 |
| Unknown or Not Reported | 0 |
| Region of Enrollment(participants) | Sleep Deprivation |
|---|---|
| United States | 12 |
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University of Colorado, Denver