Status:

COMPLETED

ICU Patient and Family Comfort Study

Lead Sponsor:

University of California, San Francisco

Collaborating Sponsors:

National Palliative Care Research Center

Conditions:

Pain

Thirst

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate family-led interventions for Intensive Care Unit (ICU) patients' symptoms (i.e., pain and thirst) that will involve ICU patients' family members in the non-pha...

Eligibility Criteria

Inclusion

  • Patient:
  • in ICU for at least 24 hours;
  • adult;
  • able to self-report;
  • pain and thirst greater than 3 on 0-10 numeric rating scale;
  • English-speaking.
  • Family member:
  • 18 years or older;
  • visits patient more than other family members;
  • closest person to patient (can be non-biological).

Exclusion

  • Patient:
  • in ICU for at less than 24 hours;
  • non-adult;
  • unable to self-report;
  • no pain and thirst greater than 3 on 0-10 numeric rating scale;
  • non-English-speaking.
  • Family member:
  • younger than 18 years;
  • visits patient less than other family members;
  • not closest person to patient.

Key Trial Info

Start Date :

February 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2010

Estimated Enrollment :

120 Patients enrolled

Trial Details

Trial ID

NCT00798941

Start Date

February 1 2009

End Date

January 1 2010

Last Update

July 8 2010

Active Locations (1)

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Page 1 of 1 (1 locations)

1

U.C. San Francisco

San Francisco, California, United States, 94143-0610

ICU Patient and Family Comfort Study | DecenTrialz