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CompletedNCT03733483SIIBUpdated Jul 12, 2021Results posted

Sleep Disruption Induced Impairments in Bone Formation

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

Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Not applicable
Ages
20 Years to 65 Years
Sex
Male
01

Study summary

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.

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Conditions studied

  • Healthy

Keywords

  • Bone
  • Sleep Restriction
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In context

Lead sponsor

University of Colorado, Denver is the lead sponsor of 1,499 studies on the registry; 315 are open to participants now.

Of its 139 completed or terminated interventional studies of FDA-regulated products, 89 (64%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 65 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

Inclusion criteria

o Adult men aged 20-65 years old who habitually sleep 7-9 hours/night.

Exclusion criteria

Exclusion Criteria:

  • Regularly go to sleep after midnight;
  • Shift work 1 year prior to study;
  • Travel >1 time zone 4 weeks prior to study or need to travel during study;
  • More than moderate activity level (>3 days of exercise per week >30 min of exercise per session);
  • Current smokers (or within the previous year of study);
  • Positive drug test at screening or laboratory admission;
  • BMI > 30 kg/m2;
  • Individuals who are concurrently participating in another research protocol that would influence their safe participation in this study. For example, participants involved in a study that requires blood draws or ingestion of experimental medication as this would increase the risk of participation in our study and/or compromise study results.
  • Any clinically significant unstable medical or surgical condition within the last year (treated or untreated), including history of a clinically significant abnormality of the neurological system (including cognitive disorders or significant head injury) or any history of seizure (including febrile seizure-sleep loss has been used clinically to induce seizures in patients with epilepsy). Given the wide range of illnesses that are encountered in medical practice, it would not be possible to provide a comprehensive list of each and every disease that could serve as grounds for exclusion for the subject. However, the following is a list of illness categories that would certainly be grounds for exclusion: Connective Tissue and Joint Disorders; Neurologic/cognitive Disorders; Musculoskeletal Disorders; Immune Disorders; Chronobiologic Disorders; Cardiovascular Disorders; Respiratory Disorders; Kidney Disorders; Infectious Diseases; Hematopoietic Disorders; Neoplastic Diseases; and Endocrine and Metabolic Diseases.
  • 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:

    • Out-of-range values measured on a fasting blood sample: glucose > 100 mg/dl, thyroid stimulating hormone \<0.5 or >5.0 uU/ml, abnormal alkaline phosphatase \<39 or >117 U/l, creatinine, or hemoglobin \<14.5 g/dl men
  • 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:

    • Subjects must demonstrate a full understanding of the requirements and demands of the study.
    • Each subject will complete psychological screening questionnaires. Exclusionary: Center for Epidemiological Studies Depression (CES-D) ≥ 16;. Subject responses to the CES-D are reviewed immediately and appropriate referrals are made if necessary.
    • Individuals who are unaware of specific psychiatric diagnoses who have a history of having been treated with antidepressants, neuroleptic medications or major tranquilizers will be excluded from study.
    • Use of anti-depressants or any like therapeutics prescribed by a physician is exclusionary
  • Individuals with any clinically significant sleep disorder; Diagnosis or symptoms of sleep disorders (history of significant parasomnia as an adult [night terrors, frequent sleep walking], insomnia, including but not limited to hypersomnias such as apnea, periodic limb movements, narcolepsy). Sleep disorders will be screened by self-report and physician interview including use of validated sleep questionnaires (PSQI, Epworth sleepiness scale, and Berlin sleep questionnaire for sleep apnea).
  • Individuals on medications known to affect bone turnover (e.g. glucocorticoids, osteoporosis medications);
  • Use of medications/supplements/drugs that impact sleep or bone metabolism (such as but not limited to sleep medications, marijuana etc.) within one month (participants can be studied at a later date).
  • Dwelling below Denver altitude (1,600 m) 6 months prior to testing;
  • Greater than moderate caffeine (>500 mg/day) or alcohol use (>14 standard drinks/week or >5 drinks in one sitting);
  • Subjects with a history of heparin-induced thrombocytopenia (HIT) or an allergy to heparin;
  • Inability to travel to the CU-AMC campus for study visits.
  • Individuals with restrictive diets (e.g., vegan)
  • Individuals with 25OHD \< 20 ng/mL;
  • Individuals with eGFR \< 60 mL/min/1.73m2 as this is known to affect CTX measurements;
  • T-score ≤ -2.5 (men ≥50 years old) or Z-score \< -2.0 (men \<50 years old) for bone mineral density (BMD) at the L-spine, femoral neck, or total hip on baseline DXA as compared to the DXA machine's normative database;
  • Symptoms of active illness (e.g., fever); note that subject can be studied at a later date.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
12 participants (actual)

Study arms

  • Experimental
    Sleep Deprivation

    Behavioral: Sleep Deprivation

Interventions

  • BehavioralSleep 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.

06

What researchers measure

Primary outcomes

  1. 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.

Secondary outcomes

  1. 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.

07

Results

Posted Jul 12, 2021
Limitations and caveats
1) A protocol deviation resulted in slightly longer sleep duration on one night in one participant. Results were unchanged when data were re-analyzed without data from that participant. 2) This data was from a small cohort of young, healthy, physically active men. 3) Activity restrictions imposed during sleep restriction may not accurately reflect activity during real-life sleep restriction. 4) Study diets provided may not accurately replicate real-life changes in diet due to sleep restriction.

Participant flow

Participant flow — Overall Study
MilestoneSleep Deprivation
Started12
Completed12
Not completed0

Outcome measures

PrimaryChange 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.
Reported as:
Mean · ng/mL
Change in Serum Pro-collagen 1 Intact N-terminal Propeptide (P1NP)
ng/mLSleep Deprivation
Baseline72.1 ± 4.4
Sleep Restricted67.4 ± 4.4
Statistical analysis
  • Sleep Deprivation · Mixed Models Analysis · p = 0.53
SecondaryChange 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.
Reported as:
Mean · ng/mL
Change in Serum C-telopeptide of Type 1 Collagen (CTX)
ng/mLSleep Deprivation
Baseline0.197 ± 0.05
Sleep Restricted0.459 ± 0.06
Statistical analysis
  • Sleep Deprivation · Mixed Models Analysis · p = 0.10

Adverse events

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.

Adverse event summary by group
GroupDeathsSeriousOther
Sleep Deprivation0/12 (0%)0/12 (0%)2/12 (16.7%)
Most frequent other events
Most frequent other events
EventSleep Deprivation
Dry eyesEye disorders1/12
IrritationSkin and subcutaneous tissue disorders1/12

Baseline characteristics

Age, Categorical
Age, Categorical(Participants)Sleep Deprivation
<=18 years0
Between 18 and 65 years12
>=65 years0
Age, Continuous
Age, Continuous(years)Sleep Deprivation
Mean28.3 ± 5.7
Sex: Female, Male
Sex: Female, Male(Participants)Sleep Deprivation
Female0
Male12
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Sleep Deprivation
Hispanic or Latino0
Not Hispanic or Latino12
Unknown or Not Reported0
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Sleep Deprivation
American Indian or Alaska Native0
Asian4
Native Hawaiian or Other Pacific Islander0
Black or African American2
White6
More than one race0
Unknown or Not Reported0
Region of Enrollment
Region of Enrollment(participants)Sleep Deprivation
United States12
08

Study locations

1 site
  • Clinical & Translational Research Centers (CTRC) UCHealth
    Aurora, Colorado 80045, United States
09

References and documents

Publications

  • Swanson CM, Shea SA, Wolfe P, Cain SW, Munch M, Vujovic N, Czeisler CA, Buxton OM, Orwoll ES. Bone Turnover Markers After Sleep Restriction and Circadian Disruption: A Mechanism for Sleep-Related Bone Loss in Humans. J Clin Endocrinol Metab. 2017 Oct 1;102(10):3722-3730. doi: 10.1210/jc.2017-01147. PubMed 28973223 ↗
  • Swanson CM, Shanbhag P, Tussey EJ, Rynders CA, Wright KP Jr, Kohrt WM. Bone Turnover Markers After Six Nights of Insufficient Sleep and Subsequent Recovery Sleep in Healthy Men. Calcif Tissue Int. 2022 Jun;110(6):712-722. doi: 10.1007/s00223-022-00950-8. Epub 2022 Feb 8. PubMed 35133471 ↗

Study documents

  • Protocol and statistical analysis plan · Sep 5, 2019

Documents are hosted by the registry — open the source record to download them.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03733483
Lead sponsor
University of Colorado, Denver
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Responsible party
Sponsor
First posted
Nov 7, 2018
Start date
Jan 17, 2019
Primary completion
Mar 16, 2020
Completion
Mar 16, 2020
Results posted
Jul 12, 2021
Last update
Jul 12, 2021

Study contacts

Christine Swanson, MD, MCR
principal investigator · University of Colorado, Denver

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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