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Brain Tumor Treatment Satisfaction Survey
This study is currently recruiting participants.
Verified by Methodist Healthcare, February 2009
First Received: November 13, 2007   Last Updated: February 3, 2009   History of Changes
Sponsored by: Methodist Healthcare
Information provided by: Methodist Healthcare
ClinicalTrials.gov Identifier: NCT00557375
  Purpose

Patients with recent diagnosis and treatment of a brain tumor will complete a short questionnaire concerning the patient's quality of life and emotional state since receiving treatment. Caregivers will complete a one-page questionnaire concerning the patient's quality of life and emotional state since receiving treatment.


Condition
Brain Tumors

MedlinePlus related topics: Brain Cancer Cancer Caregivers
U.S. FDA Resources
Study Type: Observational
Study Design: Case-Only, Cross-Sectional
Official Title: Treatment Satisfaction Survey for Brain Tumor Patients and Their Caregivers

Further study details as provided by Methodist Healthcare:

Primary Outcome Measures:
  • Overall satisfaction and emotional impact of treatments in patients who have undergone therapy(s)for brain tumors. [ Time Frame: (greater than or equal to 3 months) from first treatment for brain tumor ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Observational data about the treatment course and emotional well-being of the brain tumor patient as provided by the caregiver. [ Time Frame: (Greater than or equal to 3 months) from first treatment for brain tumor ] [ Designated as safety issue: No ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 700
Study Start Date: June 2007
Estimated Study Completion Date: November 2009
Groups/Cohorts
1
Brain tumor patients
2
Caregivers of brain tumor patients

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Brain tumor patients and their caregivers

Criteria

Inclusion Criteria:

  • Patients who are between 3 months and one year out from treatment for their brain tumor
  • Karnofsky Performance Status (KPS) >= 60
  • Age 18 years or over, any gender, any race
  • "patient caregivers will be individuals who provide the most day-to-day care for their respective brain tumor patients

Exclusion Criteria:

  • No exclusions
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00557375

Contacts
Contact: Allen Redmond, RN, BSN 901-259-5314 aredmond@semmes-murphey.com

Locations
United States, Tennessee
Methodist University Hospital Recruiting
Memphis, Tennessee, United States, 38104
Principal Investigator: Allen K. Sills, MD            
Sponsors and Collaborators
Methodist Healthcare
Investigators
Principal Investigator: Allen K. Sills, MD Methodist Healthcare
  More Information

No publications provided

Responsible Party: Methodist Healthcare ( Allen Sills, MD )
Study ID Numbers: MHIRB 2007-036
Study First Received: November 13, 2007
Last Updated: February 3, 2009
ClinicalTrials.gov Identifier: NCT00557375     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Methodist Healthcare:
Brain Tumors
Survey

Study placed in the following topic categories:
Brain Neoplasms
Central Nervous System Diseases
Central Nervous System Neoplasms
Brain Diseases
Nervous System Neoplasms

Additional relevant MeSH terms:
Brain Neoplasms
Neoplasms
Neoplasms by Site
Nervous System Diseases
Central Nervous System Diseases
Central Nervous System Neoplasms
Brain Diseases
Nervous System Neoplasms

ClinicalTrials.gov processed this record on May 07, 2009