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

NCT01983254 · ClinicalTrials.gov registry record · NA

Improving Psychological Distress Among Critical Illness Survivors and Their Caregivers

A NA study, sponsored by Duke University.

Completed
Registry status
NA
Development phase
417
Enrollment target

NCT01983254: Completed NA study, sponsored by Duke University.

NCT01983254 is a NA study that has completed, run by Duke University. The registered enrollment target is 417 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01983254, a NA study, has completed, sponsored by Duke University.

COMPLETED
Registry status
NA
Development phase
417 participants
Enrollment target

Study Summary

Patients who receive life support in intensive care units commonly suffer from persistent depression, anxiety, and post-traumatic stress disorder (PTSD) symptoms after discharge. We are trying to learn which is a better way to manage this distress: a telephone-based adaptive coping skills training program or an educational program.

Primary Outcome

Hospital Anxiety and Depression Scale (HADS) questionnaire: The HADS is a fourteen item scale. Seven of the items relate to anxiety and seven relate to depression. The anxiety and depression subscales each range from 0 to 21, with higher scores indicating higher anxiety/depression complains. Patients were defined as having anxiety or depression or both if the score was 8 or more in the corresponding subscale. The 3 month measure is primary outcome timing, though changes at 6 months will be teste

Interventions

  • BEHAVIORAL coping skills training
  • OTHER education program

Trial Details

FieldValue
Enrollment Target 417 participants
Start Date 2013-10
Est. Completion 2016-04
Phase NA
Duke University

1,725 total trials

What the finished NCT01983254 record still lists

NCT01983254 is an interventional study that assigns participants to a tested intervention. The registered 417 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which coping skills training is the first listed.

NCT01983254 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01983254 about?

NCT01983254 is a clinical study titled "Improving Psychological Distress Among Critical Illness Survivors and Their Caregivers". Patients who receive life support in intensive care units commonly suffer from persistent depression, anxiety, and post-traumatic stress disorder (PTSD) symptoms after discharge. We are trying to learn which is a better way to manage this distress: a telephone-based adaptive coping skills training p...

What is the current status of trial NCT01983254?

This trial is currently completed. It is a NA study. The enrollment target is 417 participants. The study started on 2013-10. Estimated completion is 2016-04.

What interventions are being tested in trial NCT01983254?

The interventions under investigation include: coping skills training (BEHAVIORAL), education program (OTHER).

Who is sponsoring clinical trial NCT01983254?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01983254's enrollment target sits among peer trials

417 241st of 2000 higher than 1,760 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

  • NCT06169735 · 417 participants · Phase 4

    Does Fluorescence With or Without Indocyanine Green Improve Parathyroid Identification and Preservation

  • NCT06699901 · 417 participants

    Antibiotic Concentrations After MassivE Transfusion Study

  • NCT03135886 · 418 participants · NA

    Project I Test: Implementing HIV Testing in Opioid Treatment Programs

  • NCT03527537 · 416 participants · Phase 4

    Gestational Diabetes and Pharmacotherapy (GAP)

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 NCT01983254, the US trial registry maintained by the National Library of Medicine. NCT01983254 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.