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

NCT02063737 · ClinicalTrials.gov registry record · Early Phase 1

SleepTrackTXT Feasibility and Pilot Study

A Early Phase 1 study, sponsored by University of Pittsburgh.

Completed
Registry status
Early Phase 1
Development phase
100
Enrollment target

NCT02063737: Completed Early Phase 1 study, sponsored by University of Pittsburgh.

NCT02063737 is a Early Phase 1 study that has completed, run by University of Pittsburgh. The registered enrollment target is 100 participants, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (89% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02063737, a Early Phase 1 study, has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
Early Phase 1
Development phase
100 participants
Enrollment target

Study Summary

Aim 1: To determine if real-time assessments of perceived sleepiness and fatigue using text-messaging impacts an emergency medicine clinician's Attitudes, Perceived Norms, Self-Efficacy, Alertness Habits, Perceived Importance of Fatigue, Knowledge of Sleepiness/Fatigue, and Perceptions of Environmental Constraints regarding behaviors that can improve alertness during shift work. Aim 2: To determine if text-messaging emergency care workers fatigue-reduction strategies in real-time at the start and during shift work reduces worker perceived sleepiness and fatigue at the end of shift work.

Primary Outcome

Self-reported fatigue based on scale ranging from 0 (Not At All) to 5 (Very Much).

Interventions

  • BEHAVIORAL Text-message assessments only
  • BEHAVIORAL Text-message interventions for high level fatigue

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2014-01
Est. Completion 2014-06
Phase Early Phase 1
University of Pittsburgh

1,238 total trials

What the finished NCT02063737 record still lists

NCT02063737 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, above the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (89% higher).

The record links to 0 conditions, and to 2 interventions - of which Text-message assessments only is the first listed.

NCT02063737 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02063737 about?

NCT02063737 is a clinical study titled "SleepTrackTXT Feasibility and Pilot Study". Aim 1: To determine if real-time assessments of perceived sleepiness and fatigue using text-messaging impacts an emergency medicine clinician's Attitudes, Perceived Norms, Self-Efficacy, Alertness Habits, Perceived Importance of Fatigue, Knowledge of Sleepiness/Fatigue, and Perceptions of Environmen...

What is the current status of trial NCT02063737?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 100 participants. The study started on 2014-01. Estimated completion is 2014-06.

What interventions are being tested in trial NCT02063737?

The interventions under investigation include: Text-message assessments only (BEHAVIORAL), Text-message interventions for high level fatigue (BEHAVIORAL).

Who is sponsoring clinical trial NCT02063737?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02063737's enrollment target sits among peer trials

100 184th of 2000 higher than 1,782 of 2,000 other Early Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Early Phase 1 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

  • NCT01048281 · 100 participants

    Clinical & Pathological Studies of Upper Gastrointestinal Carcinoma

  • NCT01161199 · 100 participants

    The Use of Leukapheresis to Support HIV Pathogenesis Studies

  • NCT01327690 · 100 participants · Early Phase 1

    Mental Health in Veterans and Families After Group Therapies

  • NCT01730781 · 100 participants

    Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02063737, the US trial registry maintained by the National Library of Medicine. NCT02063737 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.