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| Sponsor: | M.D. Anderson Cancer Center |
|---|---|
| Collaborator: |
National Cancer Institute (NCI) |
| Information provided by (Responsible Party): | M.D. Anderson Cancer Center |
| ClinicalTrials.gov Identifier: | NCT00895024 |
Purpose
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:
| Condition | Intervention |
|---|---|
|
Advanced Cancer |
Behavioral: Phone Interview/Questionnaire |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Caregiver Assessments of the Quality of Home Hospice Care: A Comparison Across 3 Ethnic Groups (A Preliminary Study) |
| Estimated Enrollment: | 128 |
| Study Start Date: | April 2009 |
| Estimated Primary Completion Date: | April 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Caregivers |
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Bereaved family caregivers who completed their participation in the UT MDACC parent protocol (2006-0494) and have lost their loved one within 3-23 months. Caregivers who participated in the parent grant met the inclusion/exclusion criteria of the parent grant.
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Isabel Torres, MPH, DRPH | 713-563-4125 |
| United States, Texas | |
| UT MD Anderson Cancer Center | Recruiting |
| Houston, Texas, United States, 77030 | |
| Principal Investigator: Isabel Torres, MPH, DRPH | |
| Principal Investigator: | Isabel Torres, MPH, DRPH | UT MD Anderson Cancer Center |
More Information
| Responsible Party: | M.D. Anderson Cancer Center |
| ClinicalTrials.gov Identifier: | NCT00895024 History of Changes |
| Other Study ID Numbers: | 2009-0031 |
| Study First Received: | May 5, 2009 |
| Last Updated: | November 23, 2011 |
| Health Authority: | United States: Institutional Review Board |
|
Caregiver Questionnaire Home Hospice Care Family Evaluation of Hospice Care FEHC |
The Texas Revised Inventory of Grief TRIG Cross-ethnic differences Parenteral Hydration Grief |
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Neoplasms |