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Mobile Mindfulness to Improve Psychological Distress After Critical Illness

NCT02701361 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2018-02-07

Study results available
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Summary

Many survivors of the intensive care unit (ICU) suffer from persistent symptoms of depression, anxiety, and post-traumatic stress disorder (PTSD). In this study, the investigators will test the impact of mindfulness to address this distress.

Conditions

  • Psychological Distress
  • Depression
  • Anxiety
  • Post-traumatic Stress Disorder
  • Informal Caregivers
  • Family Members

Interventions

BEHAVIORAL

mobile mindfulness

Receives audiovisual mindfulness content via internet plus call depending on symptoms or request.

BEHAVIORAL

standard mindfulness

Receives weekly calls from mindfulness expert for 4 weeks.

BEHAVIORAL

education

Receives web-based content about critical illness topics. Also receives two calls from study team to describe materials and answer questions about materials.

Sponsors & Collaborators

Principal Investigators

  • Christopher E Cox, MD · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2017-05-01
Completion
2017-07-05

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02701361 on ClinicalTrials.gov