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CompletedNCT03774810R01Updated May 9, 2025Results posted

Partial Reinforcement II: Three Approaches to Maintenance Therapy for Chronic Insomnia

A Phase 4 interventional study of Zolpidem tartrate in Insomnia and Insomnia Chronic, sponsored by University of Pennsylvania. Completed at 1 site in United States. Open to participants aged 40 Years to 85 Years. Per ClinicalTrials.gov, last updated 2025-05-09.

Sponsored by University of Pennsylvania · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
197
Allocation
Randomized
Ages
40 Years to 85 Years
Sex
All
01

Study summary

The study is a three phase sequential study of the medical treatment of insomnia with zolpidem. All participating subjects will receive one month of standard nightly treatment. If the subject has a positive treatment response they continue in the study and are randomized to one of four conditions: intermittent dosing (3-5 pills week, full dose), or one of three variable dose conditions (nightly pill use where any given pill is a variable dose). Standard treatment will last for 4 weeks. The experimental phase will extend over two periods. The first period will last for 12 weeks. The second period will last for 36 weeks. Both periods include:

  • Taking a pill 30 minutes prior to bedtime.

In one case, this will involve taking 3-5 pills per week. In the remaining condition pills will be taken on each and every night. Depending on the specific group that the subject is assigned to, they will either receive 10mg or 5mg of zolpidem (variable by age and sex) or a variable dose of zolpidem on a nightly basis (range from 0 mg to 10 mg per night).

  • Completing a sleep diary each day;
  • Completing 6 to 7 questionnaires each week;
  • A monthly visit to Penn to return your medication foil packs and to receive a new foil pack with the next month of medication.

During Phases 3\&4, the subject will be asked to undergo quarter annual physicals so that we can optimally track their health and wellbeing. The physicals will involve standard vitals measures (e.g., temperature, blood pressure, height and weight, etc.) and, based on the judgement of the research clinician, may involve an EKG and blood and urine chemistries.

If the subject does not experience a treatment response or (following a treatment response) experiences a relapse of insomnia, they will not continue in the study but will be given the opportunity to be treated with Cognitive Behavioral Therapy for Insomnia (CBT-I) at no cost. Assessments of the subjects clinical status will be based on your daily sleep diaries and weekly questionnaires.

Read the detailed description

Phase-1: Initial Evaluation.

This evaluation occurs at the offices of the Behavioral Sleep Medicine Program (Suite 670, 3535 Market Street Philadelphia, PA 19104) and lasts about 1 to 2 hours. Procedures include:

  • Completing forms asking questions about your sleep, mood, alcohol use, medical history, your current medications, and background questions about your age, race, and education.
  • The provision of your consent to contact your primary care provider to gain their assent (agreement) that you may participate in the trial safely.

The information obtained during the initial assessment will be used to see if you are eligible to participate in this study. If you are determined ineligible, you will not be able to continue in the study but will be provided with a referral if appropriate.

NOTE: This study will be using an Internet Data Portal (IDP) system to collect most questionnaire data. The IDP is a Research Electronic Data Capture and is a secure web application. It is a password protected site located on Penn's servers in which the data will live in a database online where only qualified research personnel can access it. During the initial evaluation you will be introduced to this system and provided with a username and password. The study staff will assist you in filling out the questionnaires using this IDP system.

Phase-2: Baseline Period.

This phase lasts 14 days. Your participation includes:

  • Completing daily sleep diaries at home. The online diary form requires about 5 minutes each day to complete.
  • Completing 6 to 7 forms asking questions about your medical symptoms, and sleep each week of the baseline period. These online questionnaires require about 15 minutes to complete.
  • Abstaining from the use of any medication or over the counter product that is used expressly for the purpose of helping you fall or stay asleep (e.g. trazadone/Desyrel, melatonin, Nyquil, Tylenol PM, Benadryl, etc.). If you choose to discontinue your current sleep medication to participate in our study, please do this in consultation with the clinician that prescribed your sleep medication. Please note that discontinuation of your current sleep medication will make it necessary to extend the baseline component of our study by at least two weeks. Should the sleep diaries indicate that your insomnia is not of the type, severity, or frequency required for the study, you will not be able to continue in the study but will be provided with a referral. This referral will be for the Penn Sleep Disorder Center. If you or study personnel deem your two weeks to be unusual, you may be offered the chance to repeat the baseline period.

Phase-3: Sleep Lab Study (polysomnography) or Home Sleep Apnea Test (HSAT). You will undergo a polysomnography study or an HSAT to determine if you are eligible to continue in the study. During the pandemic all sleep tests will be administered at home. After the pandemic, the study investigators will decide which type of study you will receive. Both sleep assessments will last for 1 night.

The HSAT equipment will be shipped to your house. A member of the study team will contact you to go over proper use instructions. On the night of the test, you can go to bed at your regular bedtime. Prior to bedtime, you will attach the sensor(s) as instructed and start the test. Upon waking up, you will stop the test and remove the sensor(s). On the day immediately following the sleep test, you will ship the device back in the prepaid shipping envelope Procedures for the polysomnography study are: you will be asked to arrive at the sleep lab located at the Hospital of the University of Pennsylvania (HUP) at the cross streets of 34th and Spruce by 7 P.M. for a polysomnographic study (PSG). Upon arrival, to ensure for accurate laboratory measurements, urine toxicology screens may be performed to rule out illegal substance use. These data are acquired to explain abnormal findings on the PSG. Following the sleep study, it will be determined whether a repeat study is necessary based on the findings both from the clinical chemistries and the polysomnography. If a repeat study is necessary, one of the project investigators will discuss the issue of substance use with you to: (1) determine if the clinical chemistries' finding was an error (for example poppy seeds led to a positive screen) or (2) gain your willingness to refrain from substance use for the second PSG and for the remainder of the study. If you screen positive a second time, your participation will be discontinued.

The specific procedure for a PSG requires that you have a set of sensors placed on your face, scalp, and body by a technician. All the sensors are attached with surgical tape, paste and glue. The sensors on your face are attached on your left and right temple, cheek bone and under your nose. The sensors on the temple and cheek bone measure eye movements associated with falling asleep and dreaming. The sensors under your nose measure airflow through your mouth and nose. The sensors on your scalp measure brain waves during sleep. The sensors on the body are placed above the collar bones and over the calf muscles. The sensors over the collar bones measure heart muscle activity. The sensors over the calf muscles measure muscle activity from the legs. In addition, a strap will be placed around your chest and abdomen to measure respiration.

After you have been connected to the equipment, you are expected to stay in bed until final wake time the next morning, except for bathroom breaks. You will be visually monitored by the lab technicians by remote video. In the morning, you will be awakened by the technician (if needed), be unhooked from the equipment, and then allowed to shower, dress, and eat before leaving. You will be free to go about your normal schedule for the rest of the day.

If the in-lab PSG sleep or HSAT study finds evidence of a sleep disorder other than insomnia, such as sleep apnea, you will not be able to continue in the study but will be provided with a referral.

Phase-4: Standard Treatment. All participating subjects will receive one month of standard nightly treatment. If you have a positive treatment response you will remain in the study and be randomized to one of the following treatment conditions: nightly dosing, intermittent dosing (1-3 pills week, full dose), or one of two variable dose conditions (nightly pill use where any given pill is a variable dose). The assignment of condition will be accomplished by a process that is the same as the flip of a coin and neither you nor the study personnel will know which condition you have been assigned to (this is referred to as a "double blind" study). You will have an equal chance of being randomized to each of the 4 study arms. In the case of an emergency, the blind will be broken and the study doctor and clinicians associated with your care will be informed of which dosing condition you were assigned to.

Standard treatment will last for 4 weeks. The experimental phase will extend over two periods. The first period will last for 12 weeks. The second period will last for 36 weeks.

Both periods include:

  • Taking a pill 30 minutes prior to bedtime. In one case, this will involve taking 1-3 pills per week. In the remaining conditions, pills will be taken on each and every night. Depending on the specific group you are assigned to, you will either receive 10mg or 5mg of zolpidem (variable by age and sex) or a variable dose of zolpidem on a nightly basis (range from 0 mg to 10 mg per night). Please note that the effect of zolpidem may be slowed if taken with or immediately after a meal.
  • Completing a sleep diary each day;
  • Completing 6 to 7 questionnaires each week;
  • A monthly visit to Penn to return your medication foil packs and to receive a new foil pack with the next month of medication.

If you do not experience a treatment response or (following a treatment response) you experience a relapse of insomnia, you will not be able to continue in the study but will be given the opportunity to be treated with Cognitive Behavioral Therapy for Insomnia (CBT-I) at no cost. Assessments of your clinical status (how your insomnia is responding to treatment) will be based on your daily sleep diaries and weekly questionnaires.

During Phase-4, you will be asked to undergo quarter annual physicals so that we can optimally track your health and wellbeing. The physicals will involve standard vital measures (e.g., temperature, blood pressure, height and weight, etc.) and, based on the judgement of the research clinician, may involve an EKG and/or blood and urine chemistries.

02

Conditions studied

  • Insomnia
  • Insomnia Chronic

Keywords

  • insomnia
  • sleep
  • chronic insomnia
  • zolpidem
  • ambien
03

In context

Sleep Initiation and Maintenance Disorders

1,856 studies on the registry are indexed under Sleep Initiation and Maintenance Disorders; 594 are open to participants now.

This study's enrollment of 197 is above the median of 73 across 1,631 interventional studies indexed under Sleep Initiation and Maintenance Disorders.

Browse Sleep Initiation and Maintenance Disorders studies →

Lead sponsor

University of Pennsylvania is the lead sponsor of 1,635 studies on the registry; 239 are open to participants now.

Of its 154 completed or terminated interventional studies of FDA-regulated products, 104 (68%) have results posted.

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

04

Who can participate

Ages eligible
40 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Meet DSM-5 criteria for Insomnia Disorder, ICSD-3, and RDC criteria for Psychophysiologic Insomnia
  • Age 40-85

Exclusion criteria

Exclusion Criteria:

  • currently in treatment for insomnia
  • unstable medical or psychiatric illness
  • a history of treatment failure with zolpidem
  • discontinuation of zolpidem owing to side effects
  • current experience, or history, of parasomnias (within the last 5 years)
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
197 participants (actual)

Study arms

  • Experimental
    Continuous

    Nightly active dose (QHS). The intervention is zolpidem tartrate 5 mg or 10 mg.

    Drug: Zolpidem tartrate

  • Experimental
    Partial Reinforcement 1

    1 active dose per week with 6 placebos interspersed between the active dose. The intervention is zolpidem tartrate 5 mg or 10 mg.

    Drug: Zolpidem tartrate

  • Experimental
    Partial Reinforcement 3

    3 active doses per week with 4 placebos interspersed between the active doses. The intervention is zolpidem tartrate 5 mg or 10 mg.

    Drug: Zolpidem tartrate

  • Experimental
    Low Frequency Intermittent Dosing

    1 to 3 active doses per week, on night chosen by participant (as needed). The intervention is zolpidem tartrate 5 mg or 10 mg.

    Drug: Zolpidem tartrate

Interventions

  • DrugZolpidem tartrate

    Zolpidem Tartrate, 5mg for men older than 60 and women of all ages. 10 mg for men younger than 60.

    Also known as: zolpidem, ambien

06

What researchers measure

Primary outcomes

  1. Treatment Response (Phase 1)

    Tracking treatment response via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

    Time frame: 1 Month

  2. Insomnia Relapse (Phase 2)

    Tracking relapse via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

    Time frame: 3 months

  3. Insomnia Relapse (Phase 3)

    Tracking relapse via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

    Time frame: 9 months

Secondary outcomes

  1. Sleep Continuity (Phase 1)

    Assess sleep continuity by assessing daily sleep diary responses.

    Time frame: 1 Month

  2. Sleep Continuity (Phase 2)

    Assess sleep continuity by assessing daily sleep diary responses.

    Time frame: 3 months

  3. Sleep Continuity (Phase 3)

    Assess sleep continuity by assessing daily sleep diary responses.

    Time frame: 9 months

07

Results

Posted May 9, 2025
Limitations and caveats
The following results are preliminary and do not take into account post-randomization factors such as missing data, dropout, or adherence to the intervention regimens. Accordingly, the results are considered preliminary and will be updated on or before the new year (2025).

Participant flow

197 subjects were consented and enrolled into baseline.

Phase 1
Participant flow — Phase 1
MilestoneQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Started1150000
Completed830000
Not completed320000
Withdrew: Lack of efficacy210000
Withdrew: Withdrawal by subject90000
Withdrew: Lost to follow-up20000
Phase 2 (3 Months)
Participant flow — Phase 2 (3 Months)
MilestoneQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Started022182320
Completed013141718
Not completed09462
Withdrew: Lack of efficacy03231
Withdrew: Withdrawal by subject05231
Withdrew: Lost to follow-up01000
Phase 3 (9-month Extension of Phase 2)
Participant flow — Phase 3 (9-month Extension of Phase 2)
MilestoneQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Started013141718
Completed0991012
Not completed04576
Withdrew: Lack of efficacy03212
Withdrew: Withdrawal by subject01352
Withdrew: Withdrawn by pi due to study end.00012

Outcome measures

PrimaryTreatment Response (Phase 1)

Tracking treatment response via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

Time frame:
1 Month
Reported as:
Count of participants · Participants
Treatment Response (Phase 1)
ParticipantsQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Treatment Response (Phase 1)94————
PrimaryInsomnia Relapse (Phase 2)

Tracking relapse via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

Time frame:
3 months
Reported as:
Count of participants · Participants
Insomnia Relapse (Phase 2)
ParticipantsQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Insomnia Relapse (Phase 2)—4331
SecondarySleep Continuity (Phase 1)

Assess sleep continuity by assessing daily sleep diary responses.

Time frame:
1 Month
Reported as:
Mean · Minutes
Sleep Continuity (Phase 1)
MinutesQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Sleep Latency (SL)17.35 ± 26.09————
Wake After Sleep Onset (WASO)29.46 ± 34.82————
Early Morning Awakenings (EMA)69.07 ± 52.45————
SecondarySleep Continuity (Phase 2)

Assess sleep continuity by assessing daily sleep diary responses.

Time frame:
3 months
Reported as:
Mean · Minutes
Sleep Continuity (Phase 2)
MinutesQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Sleep Latency (SL)—21.24 ± 26.5124.56 ± 45.0221.76 ± 31.3813.03 ± 20.37
Wake After Sleep Onset (WASO)—37.51 ± 39.0744.29 ± 50.7434.20 ± 38.3122.78 ± 28.46
Early Morning Awakenings (EMA)—64.77 ± 51.7969.88 ± 57.3365.61 ± 52.5653.52 ± 36.06
SecondarySleep Continuity (Phase 3)

Assess sleep continuity by assessing daily sleep diary responses.

Time frame:
9 months
Reported as:
Mean · Minutes
Sleep Continuity (Phase 3)
MinutesQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Sleep Latency (SL)—20.32 ± 27.5129.71 ± 52.4224.32 ± 35.0011.43 ± 14.09
Wake After Sleep Onset (WASO)—34.73 ± 38.3338.10 ± 42.0937.80 ± 41.0021.25 ± 28.10
Early Morning Awakenings (EMA)—59.34 ± 44.2179.12 ± 68.4862.68 ± 48.7350.19 ± 36.49
PrimaryInsomnia Relapse (Phase 3)

Tracking relapse via assessing daily sleep continuity (sleep latency, wake after sleep onset, and early morning awakenings).

Time frame:
9 months
Reported as:
Count of participants · Participants
Insomnia Relapse (Phase 3)
ParticipantsQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Insomnia Relapse (Phase 3)—3343

Adverse events

Collected over Adverse event data was collected over a period of 13 months per subject.. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
QHS-FD (Phase 1)0/115 (0%)0/115 (0%)2/115 (1.7%)
Partial Reinforcement 1 (PR1) (Phases 2 & 3)0/22 (0%)0/22 (0%)4/22 (18.2%)
Partial Reinforcement 3 (PR3) (Phases 2 & 3)0/18 (0%)0/18 (0%)7/18 (38.9%)
Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)0/23 (0%)0/23 (0%)2/23 (8.7%)
Full Dose Nightly (QHS-FD) (Phases 2 & 3)0/20 (0%)0/20 (0%)7/20 (35%)
Most frequent other events
Showing 10 of 19
Most frequent other events
EventQHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)
Daytime SleepinessNervous system disorders0/1150/221/181/233/20
Stomach Aches/NauseaGastrointestinal disorders1/1150/222/180/230/20
DizzinessNervous system disorders1/1150/221/181/232/20
Chest DiscomfortGeneral disorders0/1150/221/180/230/20
Panic AttacksPsychiatric disorders0/1150/221/180/230/20
DyspneaRespiratory, thoracic and mediastinal disorders0/1150/221/180/230/20
HypertensionCardiac disorders0/1150/221/180/230/20
Dry MouthGeneral disorders0/1150/221/180/230/20
Worsening MoodPsychiatric disorders0/1150/221/180/230/20
PhantosmiaNervous system disorders0/1150/221/180/230/20

Baseline characteristics

All subjects received the same treatment for phase 1, so none were randomized to other conditions.

Age, Continuous
Age, Continuous(years)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
Mean56.6 ± 8.3————56.6 ± 8.3
Sex: Female, Male
Sex: Female, Male(Participants)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
Female87000087
Male28000028
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
Hispanic or Latino200002
Not Hispanic or Latino1130000113
Unknown or Not Reported000000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
American Indian or Alaska Native000000
Asian800008
Native Hawaiian or Other Pacific Islander000000
Black or African American600006
White1000000100
More than one race100001
Unknown or Not Reported000000
Region of Enrollment
Region of Enrollment(participants)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
United States115————115
Sleep Continuity
Sleep Continuity(Minutes)QHS-FD (Phase 1)Partial Reinforcement 1 (PR1) (Phases 2 & 3)Partial Reinforcement 3 (PR3) (Phases 2 & 3)Low Frequency Intermittent Dosing (IDS-FD) (Phases 2 & 3)Full Dose Nightly (QHS-FD) (Phases 2 & 3)Total
Sleep Latency31.71 ± 42.98————31.71 ± 42.98
Wake After Sleep Onset50.54 ± 50.54————50.54 ± 47.67
Early Morning Awakenings74.9 ± 56.84————74.79 ± 56.84
08

Study locations

1 site
  • University of Pennsylvania
    Philadelphia, Pennsylvania 19104, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · Apr 12, 2022
  • Informed consent form · Jun 1, 2021

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

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 9, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03774810
Lead sponsor
University of Pennsylvania
Collaborators
National Institutes of Health (NIH), National Institute on Aging (NIA)
Responsible party
Sponsor
First posted
Dec 13, 2018
Start date
Apr 15, 2019
Primary completion
Sep 30, 2024
Completion
Sep 30, 2024
Results posted
May 9, 2025
Last update
May 9, 2025

Study contacts

Michael L Perlis, PhD
principal investigator · University of Pennsylvania

Oversight

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

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