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