Experience of Brain Tumor Caregivers
The Experience of Informal Caregivers of Patients With Brain Tumors
1 other identifier
observational
40
1 country
1
Brief Summary
The objective of this study is to explore the experience of informal caregivers of patients with a primary brain tumor, identifying elements and themes of the caregiving experience specific to this population of caregivers. The aim is to describe the experience of being an informal caregiver for a patient with a primary brain tumor.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2006
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2006
CompletedFirst Submitted
Initial submission to the registry
July 13, 2006
CompletedFirst Posted
Study publicly available on registry
July 17, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2006
CompletedAugust 1, 2012
July 1, 2012
8 months
July 13, 2006
July 31, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Descriptive exploratory analysis to identify themes and describe experience of caring for a person with a primary brain tumor
1 year
Study Arms (1)
Interview + Questionnaire
Interventions
Written survey lasting approximately 30 minutes.
Eligibility Criteria
Primary informal caregiver of individual with a primary brain glioma.
You may qualify if:
- years of age or older
- Ability to speak and read English
- Diagnosis of a primary brain glioma, World Health Organization Grade II-IV (PATIENT ONLY)
- At least 3 months since time of diagnosis (PATIENT ONLY)
- Identification as the primary informal caregiver by a patient with a primary brain glioma (CAREGIVER ONLY)
- Consent to participate
You may not qualify if:
- Inability to understand the intent of the study
- Medical condition that would preclude participation in an interview lasting 30 minutes (CAREGIVER ONLY)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
U.T. M.D. Anderson Cancer Center
Houston, Texas, 77030, United States
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Loretta A. Williams, DSN
M.D. Anderson Cancer Center
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 13, 2006
First Posted
July 17, 2006
Study Start
April 1, 2006
Primary Completion
December 1, 2006
Study Completion
December 1, 2006
Last Updated
August 1, 2012
Record last verified: 2012-07