Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03322774 · ClinicalTrials.gov registry record · NA

Sleep To Reduce Incident Depression Effectively

A NA study, sponsored by Henry Ford Health System.

Completed
Registry status
NA
Development phase
1,237
Enrollment target

NCT03322774: Completed NA study, sponsored by Henry Ford Health System.

NCT03322774 is a NA study that has completed, run by Henry Ford Health System. The registered enrollment target is 1,237 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (12% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03322774, a NA study, has completed, sponsored by Henry Ford Health System.

COMPLETED
Registry status
NA
Development phase
1,237 participants
Enrollment target

Study Summary

This project will assess the effectiveness of a stepped-care model (i.e. digital Cognitive Behavioral Therapy for Insomnia (dCBT-I) followed by face-to-face CBT-I) in improving severity of insomnia and sleep outcomes in an insomnia cohort. This project will also investigate the effectiveness of this stepped-care model in prevention of major depressive disorder, and will test rumination as a mediator of treatment response.

Primary Outcome

Clinical interview by phone administered by trained personnel to determine DSM-5 major depressive disorder incidence and relapse. Major depressive disorder will specifically be determined by the structured clinical interview for DSM-5 (SCID-5) at 1- and 2-year follow-ups. Antidepressant history in the past 1 year is collected via online-administered surveys at 1- and 2-year follow-ups.

Interventions

  • BEHAVIORAL digital Cognitive Behavioral Therapy for Insomnia
  • BEHAVIORAL face-to-face Cognitive Behavioral Therapy for Insomnia
  • BEHAVIORAL Sleep Hygiene Education Control

Trial Details

FieldValue
Enrollment Target 1,237 participants
Start Date 2018-03-09
Est. Completion 2024-06-27
Phase NA
Henry Ford Health System

234 total trials

What the finished NCT03322774 record still lists

NCT03322774 is an interventional study that assigns participants to a tested intervention. Its 1,237 participants enrollment target places it among the larger protocols in the corpus, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (12% lower).

The record links to 0 conditions, and to 3 interventions - of which digital Cognitive Behavioral Therapy for Insomnia is the first listed.

NCT03322774 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03322774 about?

NCT03322774 is a clinical study titled "Sleep To Reduce Incident Depression Effectively". This project will assess the effectiveness of a stepped-care model (i.e. digital Cognitive Behavioral Therapy for Insomnia (dCBT-I) followed by face-to-face CBT-I) in improving severity of insomnia and sleep outcomes in an insomnia cohort. This project will also investigate the effectiveness of this...

What is the current status of trial NCT03322774?

This trial is currently completed. It is a NA study. The enrollment target is 1,237 participants. The study started on 2018-03-09. Estimated completion is 2024-06-27.

What interventions are being tested in trial NCT03322774?

The interventions under investigation include: digital Cognitive Behavioral Therapy for Insomnia (BEHAVIORAL), face-to-face Cognitive Behavioral Therapy for Insomnia (BEHAVIORAL), Sleep Hygiene Education Control (BEHAVIORAL).

Who is sponsoring clinical trial NCT03322774?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03322774's enrollment target sits among peer trials

1,237 82nd of 2000 higher than 1,919 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05456841 · 1,232 participants · NA

    Empathic Communication Skills (ECS) Training

  • NCT06368245 · 1,244 participants

    Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions

  • NCT05946044 · 1,230 participants · NA

    The Osteoarthritis Prevention Study

  • NCT06787937 · 1,230 participants · NA

    Communicating About Nicotine Reduction in Cigarettes

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

Source: ClinicalTrials.gov NCT03322774, the US trial registry maintained by the National Library of Medicine. NCT03322774 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.