Trial · NCT07893015
SHLH for Urban Adolescents (Efficacy Trial)
NCT07893015, Not applicable, Enrolling by invitation, Columbia University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. SHLH for Urban Adolescents (Efficacy Trial). Trials, record NCT07893015. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07893015
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- SHLH for Urban Adolescents (Efficacy Trial)
- NCT number
- NCT07893015
- Status
- Enrolling by invitation
- Phases
- Not applicable
- Enrollment
- 294 participants, estimated
- Lead sponsor
- Columbia University
- Conditions
- Poor Quality Sleep
- Interventions
- Sleeping Healthy, Living Healthy, Sleep for Teens
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | PROMIS Sleep-Related Impairment (SRI) t-score | 2 months post-intervention | This measure assess adolescent-reported sleep-related impairment. The PROMIS Sleep-Related Impairment (SRI) is an 8-item questionnaire with a standardized, metric score (mean = 50, SD = 10) that reflects the severity of daytime consequences of poor sleep, such as sleepiness, tiredness, and functional limitations, with higher scores indicating greater impairment. |
| Primary | Average length of sleep duration | 2 months post-intervention | This is an objective measure of nightly total sleep time (i.e., minutes asleep, excluding wake after sleep onset) as measured by a wrist-worn Fitbit Inspire 3. The Fitbit estimates sleep from accelerometry and photoplethysmography-derived heart rate. Fitbit data will be corroborated with a Consensus Sleep Diary (CSD). |
| Secondary | Pittsburgh Sleep Quality Index (PSQI) Global score | Up to 1 year post-intervention | This is to measure sleep quality. The PSQI consists of 19 self-rated questions that evaluate various aspects of sleep quality, categorized into seven components. Each component is scored from 0 to 3, with 0 indicating no difficulty and 3 indicating severe difficulty. |
| Secondary | PROMIS Pediatric Sleep Disturbance -- Short Form 8a | Up to 1 year post-intervention | This scale measures adolescent-reported sleep disturbances. On a 5-point likert-type scale, adolescents report the the extent to which they experienced sleep problems in the past 7 days (1 = never to 5 = always) |
| Secondary | Objective Sleep Disturbance | Up to 1 year post-intervention | Objective nightly minutes awake after sleep onset (WASO) and number of awakenings, as estimated by the Fitbit Inspire 3 from accelerometry and heart rate. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants1
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years |
|---|---|---|---|---|---|
| R61HL186023 | A School-based Intervention to Improve Sleep Health in Urban Adolescents | Bruzzese, Jean-Marie | COLUMBIA UNIVERSITY HEALTH SCIENCES | NATIONAL HEART LUNG AND BLOOD INSTITUTE | 2026 |
Source NIH RePORTER
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07893015
GET https://conductscience.org/api/trials/v1/NCT07893015/registered