Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06501690 · ClinicalTrials.gov registry record · NA
Feasibility of a Bedtime Variability Protocol
A NA study of Sleep, sponsored by Penn State University.
- Completed
- Registry status
- NA
- Development phase
- 5
- Enrollment target
- 1
- Study location
NCT06501690: Completed NA study of Sleep, sponsored by Penn State University.
NCT06501690 is a NA study of Sleep that has completed, run by Penn State University. The registered enrollment target is 5 participants, below the 4,166-participant average among 151 other Sleep trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06501690, a NA study of Sleep, has completed, sponsored by Penn State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 5 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to find out if parents and children 6-10 years old are willing and able to follow a protocol to be used to study the effects of short and/or variable sleep in children. During each of three, one-week long periods, parents will have their child follow one of the following bedtime schedules: 1) habitual bedtime; 2) 1 hour later bedtime; or 3) variable bedtime (+/- 1 hour of habitual bedtime each day). Children will wear a sleep tracker and parents will complete daily diaries. Participants will answer questions about their experiences completing the protocol.
Primary Outcome
Parents will report on the time their child went to bed
Conditions Studied
Interventions
- BEHAVIORAL Late bedtime
- BEHAVIORAL Variable bedtime
Study Locations (1)
Pennsylvania
- Pennsylvania State University - University Park
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2024-07-10 |
| Est. Completion | 2024-09-30 |
| Phase | NA |
What the finished NCT06501690 record still lists
NCT06501690 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 4,166-participant average among 151 other Sleep trials with a reported enrollment target (100% lower).
The record links to 1 condition, with Sleep appearing as the primary indexed condition, and to 2 interventions - of which Late bedtime is the first listed.
NCT06501690 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT06501690 about?
NCT06501690 is a clinical study titled "Feasibility of a Bedtime Variability Protocol". The purpose of this study is to find out if parents and children 6-10 years old are willing and able to follow a protocol to be used to study the effects of short and/or variable sleep in children. During each of three, one-week long periods, parents will have their child follow one of the following...
What is the current status of trial NCT06501690?
This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2024-07-10. Estimated completion is 2024-09-30.
What conditions does trial NCT06501690 study?
This clinical trial studies the following conditions: Sleep.
What interventions are being tested in trial NCT06501690?
The interventions under investigation include: Late bedtime (BEHAVIORAL), Variable bedtime (BEHAVIORAL).
Who is sponsoring clinical trial NCT06501690?
This trial is sponsored by Penn State University, which has 219 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06501690 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Sleep
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06501690's enrollment target sits among peer trials
5 152nd of 151 the lowest of 151 other Sleep trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Sleep trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
-
Student Exercise and Sleep Timing Study - Part 2
RECRUITING · NA
-
The Effects of Sleep on Human Microbiota: Implications for Health and Disease
RECRUITING · NA
-
The Goodnight Screen Media Study
RECRUITING · NA
-
Black Impact: The Mechanisms Underlying Psychosocial Stress Reduction in a Cardiovascular Health Intervention
RECRUITING · NA
-
The Iowa ACEs and Sleep Cohort and Manipulating Sleep in Young Adults With ACEs Studies
RECRUITING · NA
-
Shifting Sleep Timing in Teens
RECRUITING · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI