AzTrials
AzTrials

SleepNCT00777829

Memory Consolidation in Pharmacologically Enhanced Naps

A study testing zolpidem in people with Sleep, run by University of California, San Diego at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study will examine whether various drugs affecting sleep cycles can improve different kinds of memory. Read more about this study

Who is it for?
Ages 18 to 39 yearsHealthy volunteers can take part
Conditions the study is for
Sleep
What is being tested?
zolpidem
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
30 participants
Where
1 siteUnited States
Study dates
1 Sep 2008to 1 Jun 2011
Phase
Interventional
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 39 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Speaks English
  • Resides in the general San Diego community
  • Completed at least 12 years of formal education, because education may affect performance on the cognitive task

Who cannot join

  • No regular sleep-wake schedule, defined as not meeting study criteria or scoring between 31 and 69 on the Horne-Ostberg Morningness-Eveningness Questionnaire
  • Presence of a sleep disorder reported or detected on the questionnaires
  • Personal or immediate family (i.e., first degree relative) history of diagnosed significant psychopathology
  • Personal history of head injury with loss of consciousness for more than 15 minutes or with seizures
  • History of substance dependence
  • Current use of any psychotropic medications
  • Any cardiac, respiratory, or other medical condition that may affect cerebral metabolism
  • Noncorrectable vision and audition impairments

Trial locations and contacts

1 site in 1 country.

United States1 site
  • UCSD General Clinical Research Center Laboratory for Sleep and Chronobiology (GCRC-LSC)

    La Jolla, California, 92093

Other trials in United States

About this study

Official title: Understanding Memory Consolidation by Studying Pharmacologically Enhanced Naps.

This study will examine whether various drugs affecting sleep cycles can improve different kinds of memory.

Read the detailed description

Research provides evidence for strong, specific connections between sleeping and memory. This research shows that sleeping is necessary for certain types of memories to form, certain sleep stages lead to specific types of learning and memory consolidation, and naps are as effective as night-time sleep in these learning and memory processes. Current evidence also indicates that there are different types of memory and that the different types can operate and develop independently. In this study, three different memory types will be examined: perceptual, motor, and declarative memory. Perceptual memory is measured through the ability to recognize discrete stimuli; motor memory is measured through the ability to perform specific, coordinated tasks; and declarative memory is measured through the ability to recite memorized information. Different stages in the sleep cycle correlate with improvements in each of these memory processes. For instance, improvement of perceptual memory tasks is dependent on rapid eye motion (REM) sleep; motor learning is related to sleep stage 2; and declarative memory consolidation is related to short wave sleep (SWS), which includes sleep stages 3 and 4.

New drugs can target specific sleep stages and increase the amount of time people spend in those stages when they sleep. For example, the new prescription drug zolpidem increases time spent in stage 2 during sleep, and the drug sodium oxybate increases time spent in SWS. Compared to sleep impacted by either zolpidem or sodium oxybate, normal sleep has proportionally more time spent in REM. This study will use medications, or their lack, to manipulate how much time is spent in REM, stage 2, and SWS. The study will then examine whether the percentage of sleep spent in different stages affects the learning processes associated with those stages.

Participation in this study will last 6 weeks. At the outset, participants will undergo a 2-hour screening visit that will include a medical history, a physical examination, routine lab tests, urine tests for drugs and pregnancy, an electrocardiogram, and a clinical interview for mental health. Participants will also be asked to complete a series of questionnaires on subjective sleep quality, sleep quantity, and daytime sleepiness.

Participants will complete five study visits, beginning 1 week from screening and separated by 5 to 10 days to allow drug wash-out and recovery from effects of the previous visit. Each study visit will involve an overnight stay in a sleep lab. Participants will arrive at 8 PM, go to bed at 10 PM, and be awakened at 5 AM. Between 6 and 8 AM, they will undergo three different tests, each corresponding to a different type of learning and memory process: perceptual, motor, or declarative. The test will include recognizing a target image, typing a specific finger sequence on a keyboard, and verbally recalling a list of words. Participants will receive one of the study drugs or placebo at 8:30 AM and then be allowed to take a 90-minute nap between 9 and 11 AM. They will receive a different drug, different dosage, or placebo at each study visit. Between 4 and 6 PM, they will be retested on the previous three tests. While sleeping, participants will be outfitted with sensors monitoring muscle activity, eye movements, brain waves, heart and lung functioning, and-on the first night-breathing.

For the entire duration of the study, participants will wear an actigraph, which is a wristwatch-like device that monitors sleep cycles. Participants will also be required to maintain a regular sleep schedule, going to sleep and waking up in the same 2-hour window each day. They will also report on sleep schedule and caffeine, alcohol, and drug use in a daily sleep diary. Caffeine, alcohol, and drug use will be prohibited starting at noon on the day prior to each study visit.

Conditions
Sleep
Being tested
zolpidem, Placebo
Keywords
Nap, Pharmacology, Memory, Visual Learning, Verbal Memory, Motor Learning
Medical subject headings
Spatial Learning

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • zolpidemDrug

    Participants will receive one dose of 10 mg before each nap.

  • PlaceboDrug

    Participants will receive a dose of placebo before each nap.

Study groups in NCT00777829
Study groupRoleWhat they receive
zolpidem first, then placeboExperimentalParticipants received one dose of zolpidem for one nap, then had a one week washout period, followed by once dose of placebo for one nap.
Receives: Drug: zolpidem; Drug: Placebo
Placebo first, then zolpidemPlacebo comparatorParticipants received one dose of placebo for one nap, then had a one week washout period, followed by once dose of zolpidem for one nap.
Receives: Drug: zolpidem; Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pharmacological Enhancement of Specific Sleep Parameters

    Number of sleep spindles comparing placebo vs active drug. We count spindles in the EEG record.

    Measured: Two weeks

Secondary outcomes (1)
  1. Correlation of Pharmacological Interventions With Sleep-stage-specific Memory Tasks

    improvement on a verbal memory task in active drug. We measured the number of words recalled.

    Measured: two weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Oct 2008 (estimated)
  2. Study start1 Sep 2008
  3. Primary completion1 Jun 2011
  4. Study completion1 Jun 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Crossover
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00777829
Sponsor's protocol ID
K01MH080992-01
Other IDs
K01MH080992-01, 071529, DNBBS 7K-TGNB
Status last verified
Jul 2021
First submitted
20 Oct 2008
Last updated
28 Jul 2021
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing zolpidem in people with Sleep, run by University of California, San Diego at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 28 Jul 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pharmacological Enhancement of Specific Sleep Parameters (time frame: Two weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2021.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in