The Effectiveness of a Post-ICU Recovery Program on Relatives

NCT03264365 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 181

Last updated 2018-03-07

No results posted yet for this study

Summary

Relatives of intensive care patients are at risk of developing symptoms of anxiety, depression and post-traumatic stress disorder resulting in impaired health-related quality of life (HRQOL). Recovery programs have been tested, but its effectiveness is sparse. The hypothesis is that relatives to former intensive care patients will improve their HRQOL one year after intensive care. We want to determine whether relatives to former intensive care patient's benefits from a recovery programme with improved HRQOL, Sense Of Coherence (SOC) and symptoms of anxiety, depression and PTSD compared to standard care one year after intensive care.

Conditions

  • Intensive Care Unit Syndrome
  • Relatives

Interventions

BEHAVIORAL

Intervention

Intervention (plus standard care) * Patients photographs during the ICU-stay, * Written information about life after ICU * First consultation face-to-face in hospital setting at three months after ICU * Visit ICU and photographs given * Consultations as needed

Sponsors & Collaborators

  • Nordsjaellands Hospital

    collaborator OTHER
  • Herlev Hospital

    collaborator OTHER
  • Horsens Hospital

    collaborator OTHER
  • Nykøbing Falster County Hospital

    collaborator OTHER
  • Naestved Hospital

    collaborator OTHER
  • Rigshospitalet, Denmark

    collaborator OTHER
  • Aabenraa Hospital

    collaborator OTHER
  • Sonderborg Hospital

    collaborator OTHER_GOV
  • Esbjerg Hospital - University Hospital of Southern Denmark

    collaborator OTHER
  • Svendborg Hospital

    collaborator OTHER
  • Holbaek Sygehus

    lead OTHER

Principal Investigators

  • RAPIT Steering Committee · Region of Copenhagen Capital and Region of Zealand

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-15
Primary Completion
2015-12-31
Completion
2018-03-06

Countries

  • Denmark

Study Locations

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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 NCT03264365 on ClinicalTrials.gov