Skip to main content
Clinical Trials/NCT02441868
NCT02441868
Completed
N/A

Feasibility Testing of a Hospice Family Caregiver Intervention to Improve Patient Dyspnea Care

Wayne State University1 site in 1 country7 target enrollmentOctober 15, 2015
ConditionsDyspnea

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dyspnea
Sponsor
Wayne State University
Enrollment
7
Locations
1
Primary Endpoint
Change in patient respiratory comfort
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This study is a pilot test of an intervention to train family caregivers of home hospice patients about recognizing and treating shortness of breath.

Detailed Description

Shortness of breath is a prevalent symptom causing distress among patients at the end of life. In home hospice care family caregivers are expected to assist their family member with symptom management. This is often accomplished with little or no training. The investigators have developed a bundle of training materials targeted for family caregivers of home hospice patients at risk for shortness of breath. The investigators will pilot test the intervention in this clinical trial. A future randomized clinical trial is planned and the evidence from this pilot will enhance the planning of that future trial.

Registry
clinicaltrials.gov
Start Date
October 15, 2015
End Date
April 30, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Margaret Campbell

Professor

Wayne State University

Eligibility Criteria

Inclusion Criteria

  • Patient in home hospice care with an estimated survival of 3-4 weeks, at risk for dyspnea secondary to lung cancer, COPD, or heart failure.
  • Family caregiver in patient's home must speak and read English.

Exclusion Criteria

  • Patients with bulbar ALS or quadriplegia.

Outcomes

Primary Outcomes

Change in patient respiratory comfort

Time Frame: Baseline and up to four weeks until patient death

The Respiratory Distress Observation Scale will be used to measure patient respiratory comfort at enrollment (baseline), twice each week during the study until patient death.

Secondary Outcomes

  • Family caregiver burden index(Baseline and participants will be followed for an average of 4 weeks until date of death)

Study Sites (1)

Loading locations...

Similar Trials