Caregiver Assessments of the Quality of Home Hospice Care
The Objectives are to administer the Family Evaluation of Hospice Care (FEHC) questionnaire and The Texas Revised Inventory of Grief (TRIG) to caregivers previously enrolled into the parent grant and conduct supplemental analyses to:
- examine cross-ethnic differences in the caregivers' quality of hospice care assessments.
- investigate the association between parenteral hydration status of the patient and the quality of care assessments provided by the caregivers after death.
- examine the association between levels of grief (as measured by the TRIG) and the quality of hospice care assessments provided by the caregiver.
|Study Design:||Observational Model: Other
Time Perspective: Prospective
|Official Title:||Caregiver Assessments of the Quality of Home Hospice Care: A Comparison Across 3 Ethnic Groups (A Preliminary Study)|
- Survey assessment of cross-ethnic differences in caregivers' quality of hospice care [ Time Frame: 3-23 Months After Hospice Care ]
|Actual Study Start Date:||April 2009|
|Estimated Study Completion Date:||April 2019|
|Estimated Primary Completion Date:||April 2019 (Final data collection date for primary outcome measure)|
Behavioral: Phone Interview/Questionnaire
35-minute questionnaire over the phone.
Other Name: Survey
After the death of their loved-ones, caregivers will be asked to report on the care received by their care recipient and the quality of practical and emotional care provided to them by hospice by completing the 25-minute FEHC questionnaire over the phone. Caregivers will also be asked 16 additional questions to assess their attitudes and beliefs about hydration at the end of life, and a brief questionnaire to assess past and current levels of grief (TRIG). The additional questions on hydration and grief can easily be completed in less than 10 minutes over the phone. The entire interview should take no more than 35 minutes to complete.
Bereaved caregivers who have participated in the parent grant and have lost their loved one within 3-23 months will be mailed a letter from Drs. Bruera and Torres inviting them to participate in the voluntary supplemental after-death survey. The letter will include a brief description of the research study and appropriate contact information for the caregiver to call if she/he is interested in participating. The letters then will be followed up by a phone call from Dr. Torres to verify receipt of the letter. If the caregivers express their interest in participating in the study, they will be asked a few screening questions over the phone to verify their eligibility. Once found eligible for the study, a telephone verbal consent will be obtained.
Dr. Isabel Torres will conduct the phone interviews with 128 primary caregivers who had previously completed the parent grant protocol.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00895024
|United States, Texas|
|University of Texas MD Anderson Cancer Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Isabel Torres, MPH, DRPH||M.D. Anderson Cancer Center|