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Effects of Hydrocortisone, Melatonin, and Placebo on Jet Lag

Primary Purpose

Jet Lag

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Hydrocortisone
Melatonin
Placebo
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Jet Lag focused on measuring Cortisol, Jet Lag, Healthy Volunteer, HV

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

INCLUSION CRITERIA: Age greater than or equal to 18, but less than or equal to 65, male or female. Normal physical exam and laboratory results. Negative urinary pregnancy test 1 week prior to travel (pre-menopausal women). Planned eastward flight crossing 6-8 time zones between 30n and 50n latitudes. A minimum stay of 7 - 10 days abroad. Willingness and anticipated ability to comply with study procedures, including sleep and wake hours, saliva collection and questionnaire completion. Written informed consent. EXCLUSION CRITERIA: BMI less than or equal to 20 or greater than or equal to 30 kg/m. Current psychiatric or seizure disorder. Current sleep disorder as assessed by presence of sleep apnea, daytime napping of more than 20 minutes, chronic fatigue. History of Cushing's syndrome. Serious chronic medical condition. Current drug or alcohol abuse. SGOT or SGPT greater than three-fold normal. Current pregnancy or lactation. Current use of CPAP. Chronic use of beta-blockers (which inhibit melatonin secretion), anti-epileptic agents, anticoagulants, fluvoxamine, nifedipine or soporific or sleep-inducing agents (including benzodiazepines, melatonin), or glucocorticoids. Fasting blood glucose greater than 110 mg/dL or known diabetes.

Sites / Locations

  • National Institutes of Health Clinical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Placebo Comparator

Arm Label

Combination

Hydrocortisone

Melatonin

Placebo

Arm Description

Both HC 30 and ML 5 will be administered

30mg Hydrocortisone will be administered

5 mg Melatonin will be administered

Placebo

Outcomes

Primary Outcome Measures

improvement in jet lag symptoms
Patients will report jet lag symptoms via questionnaire

Secondary Outcome Measures

salivary cortisol level
salivary cortisol at bedtime will be measured

Full Information

First Posted
November 23, 2004
Last Updated
October 6, 2023
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00097474
Brief Title
Effects of Hydrocortisone, Melatonin, and Placebo on Jet Lag
Official Title
The Effects of Hydrocortisone, Melatonin, and Placebo on Symptoms of Jet Lag
Study Type
Interventional

2. Study Status

Record Verification Date
October 4, 2023
Overall Recruitment Status
Completed
Study Start Date
December 21, 2004 (Actual)
Primary Completion Date
January 6, 2006 (Actual)
Study Completion Date
November 14, 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study will examine the effects of cortisol (hydrocortisone), melatonin, a combination of cortisol and melatonin, and placebo (an inactive substance) on jet lag symptoms. Jet lag is a term used to describe symptoms people commonly experience after rapid travel across several time zones. The cause of jet lag is not known, but various hormones, including cortisol and melatonin, have a day-to-night pattern of secretion and play a role in maintaining the body's internal rhythms. This study will test whether taking cortisol, melatonin, or both can help re-establish the body's day-night cycle and result in less jet lag. People between 18 and 65 years of age who are planning a non-stop eastward flight with the following characteristics may be eligible for this study: Crossing six to eight time zones (6 to 8 hours difference between Eastern Standard Time and the destination) Destination between 30 and 50 latitudes (approximately Cairo to London) Evening flight (5 PM to midnight) with morning arrival Remaining abroad at least 4-10 days Candidates must have a body mass index (BMI) between 20 and 30 kg/M (not too thin and not overweight) and must not be taking medicines that affect sleep or cortisol or melatonin levels. Prospective participants are screened with a medical history, blood tests, and check of blood pressure, height, and weight. Pre-flight Procedures Participants keep a sleep journal 3 days before the flight. For 1 day within 3 days of the flight they fill out jet lag and sleepiness questionnaires and collect morning and bedtime saliva samples for measurement of cortisol and melatonin. The saliva is collected by chewing on two small cotton pads and spitting them into a tube. Premenopausal women provide a urine sample the week before the flight to test for pregnancy. On the day of the flight, the participants do not collect saliva or fill out sleep logs or questionnaires. They are given two bottles with study medication. One bottle, labeled "AM," contains either hydrocortisone or placebo; the other, labeled "PM," contains either melatonin or placebo. Post-flight Procedures Upon arriving at their destination in the morning, participants obtain a saliva sample and take one of the capsules in the "AM" bottle. At bedtime, they collect saliva and then take one of the "PM" capsules. They repeat the medication doses for a total of 4 days and repeat the saliva collections on days 2 through 4, 7 and 10 after arrival. In addition, participants complete jet lag and sleep questionnaires in the morning, afternoon, and just before bedtime on the day of arrival and on days 2 through 4, 7 and 10. After they return from their trip, participants are seen at the NIH Clinic to bring in their saliva specimens and review their questionnaires with study investigators.
Detailed Description
Jet lag resulting from rapid flight across several time zones is a common complaint of travelers. The symptoms of jet lag are primarily described as daytime sleepiness, fatigue, and impaired mental efficiency and can also include weakness and irritability. It is considered to be due to the desynchronization between the internal circadian rhythm and the new local day-night cycle at the traveler s destination. A means of rapidly resynchronizing the circadian rhythm to the local time would benefit people who suffer severely from this syndrome. What actually underlies jet lag is a question that has not been fully answered. Various endogenous hormones, including cortisol and melatonin, have a natural circadian rhythmicity and play a role in maintaining the body s internal clock. Cortisol is produced by the hypothalamic- pituitary-adrenal axis in a circadian manner and in response to stress. Normal cortisol has a diurnal rhythm with a maximum level in the morning and a nadir during the night. While a time shift does not change the total daily amount of cortisol that is secreted, the temporal organization of the cortisol secretions is disrupted and the circadian rhythm does not re-entrain for several days. Thus, the first few mornings in a new time zone can be considered relatively cortisol-deficient because the traveler does not experience the peak of cortisol at the time of awakening. Taking exogenous glucocorticoids at the proper time may help re-entrain the circadian rhythm faster and result in less jet lag. Melatonin is a hormone that is secreted nocturnally by the pineal gland. Exposure to bright light diminishes its release while darkness triggers it. A recent meta-analysis has shown that taking melatonin can alleviate symptoms of jet lag. The aim of the present study is an attempt for the first time to attenuate jet lag symptoms with hydrocortisone, melatonin, a combination of both hydrocortisone and melatonin or placebo. Forty-eight normal volunteers will be randomized in blocks of eight to one of four treatment arms: hydrocortisone (25 mg) alone, melatonin (5 mg) alone, hydrocortisone (25 mg) and melatonin (5 mg) in combination, and placebo. Volunteers will travel in an eastwardly direction across 6-8 time zones. Upon morning arrival at the new destination, volunteers will obtain a saliva sample and then take 25 mg hydrocortisone (or placebo). At the target bedtime of (10 pm to midnight local time) they will take 5 mg of melatonin (or placebo). Volunteers will wake up at 7 am-10:30 am (local time) and take 25 mg hydrocortisone (or placebo). Subjects will repeat these dosages for 3 days for a total of four days. Participants also will obtain salivary samples of cortisol and melatonin on awakening and at bedtime on one day before travel and at the new destination for days 1 - 4, 7 and 10 after arrival. The primary outcome measure will be subjective rating of jet lag and components or correlates of this such as fatigue and daytime tiredness. Subjects will keep sleep logs and fill out a symptoms questionnaire daily for 3 days before and 4 days after the flight and on days 7 and 10. Secondary outcomes will be the measurement of salivary cortisol and melatonin. The data obtained from this study will provide an assessment of effective treatment of jet lag syndrome and will provide a better understanding of the role of hormones in the disruption of the circadian rhythm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Jet Lag
Keywords
Cortisol, Jet Lag, Healthy Volunteer, HV

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
57 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Combination
Arm Type
Experimental
Arm Description
Both HC 30 and ML 5 will be administered
Arm Title
Hydrocortisone
Arm Type
Experimental
Arm Description
30mg Hydrocortisone will be administered
Arm Title
Melatonin
Arm Type
Experimental
Arm Description
5 mg Melatonin will be administered
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone
Intervention Description
Hydrocortisone will be given alone or in combination with Melatonin to see if symptoms of jet lag are alleviated
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
Melatonin will be given alone or in combination with Hydrocortisone to see if symptoms of jet lag are alleviated
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
improvement in jet lag symptoms
Description
Patients will report jet lag symptoms via questionnaire
Time Frame
10 days
Secondary Outcome Measure Information:
Title
salivary cortisol level
Description
salivary cortisol at bedtime will be measured
Time Frame
10 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA: Age greater than or equal to 18, but less than or equal to 65, male or female. Normal physical exam and laboratory results. Negative urinary pregnancy test 1 week prior to travel (pre-menopausal women). Planned eastward flight crossing 6-8 time zones between 30n and 50n latitudes. A minimum stay of 7 - 10 days abroad. Willingness and anticipated ability to comply with study procedures, including sleep and wake hours, saliva collection and questionnaire completion. Written informed consent. EXCLUSION CRITERIA: BMI less than or equal to 20 or greater than or equal to 30 kg/m. Current psychiatric or seizure disorder. Current sleep disorder as assessed by presence of sleep apnea, daytime napping of more than 20 minutes, chronic fatigue. History of Cushing's syndrome. Serious chronic medical condition. Current drug or alcohol abuse. SGOT or SGPT greater than three-fold normal. Current pregnancy or lactation. Current use of CPAP. Chronic use of beta-blockers (which inhibit melatonin secretion), anti-epileptic agents, anticoagulants, fluvoxamine, nifedipine or soporific or sleep-inducing agents (including benzodiazepines, melatonin), or glucocorticoids. Fasting blood glucose greater than 110 mg/dL or known diabetes.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lynnette K Nieman, M.D.
Organizational Affiliation
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Institutes of Health Clinical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
3085768
Citation
Arendt J, Aldhous M, Marks V. Alleviation of jet lag by melatonin: preliminary results of controlled double blind trial. Br Med J (Clin Res Ed). 1986 May 3;292(6529):1170. doi: 10.1136/bmj.292.6529.1170. No abstract available.
Results Reference
background
PubMed Identifier
11083601
Citation
Buxton OM, Copinschi G, Van Onderbergen A, Karrison TG, Van Cauter E. A benzodiazepine hypnotic facilitates adaptation of circadian rhythms and sleep-wake homeostasis to an eight hour delay shift simulating westward jet lag. Sleep. 2000 Nov 1;23(7):915-27.
Results Reference
background
PubMed Identifier
10704520
Citation
Cho K, Ennaceur A, Cole JC, Suh CK. Chronic jet lag produces cognitive deficits. J Neurosci. 2000 Mar 15;20(6):RC66. doi: 10.1523/JNEUROSCI.20-06-j0005.2000.
Results Reference
background
Links:
URL
https://clinicalstudies.info.nih.gov/cgi/detail.cgi?B_2005-CH-0037.html
Description
NIH Clinical Center Detailed Web Page

Learn more about this trial

Effects of Hydrocortisone, Melatonin, and Placebo on Jet Lag

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