Return to List

Study Summary
No. 2008-0080:.......Head And Neck; Skin......Michelle C. Fingeret......Behavioral Science
.
Study Summary Title
Study Summary
Number:
2008-0080
Study Title:Body Image Functioning Among Surgically Treated Patients with Head and Neck Cancer
.
Physician New Patient Referral
Name:Michelle C. FingeretPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Behavioral ScienceReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-563-8032
Contact us about clinical trials
.
General Information
Disease Group:Head And Neck
Skin
Supported By:N/A
Phase of Study:N/AReturn
Visit:
N/A, We are collecting data at a single time point for each participant.
Treatment
Agents:
NoneHome Care:N/A
Treatment Loc:Only at MDACC
Estimated
Length of Stay
in Houston:
N/A
Description/
Intervention:
The goal of this research study is to learn how patients with head and neck
cancer feel about bodily changes caused by cancer.
.
Study Objectives / Outcomes
The purpose of this study is to obtain descriptive information about the nature and extent of body image concerns among surgical patients with head and neck cancer, satisfaction with care received regarding body image issues, and interest in psychosocial services targeting body image disturbance. Findings from this study provide important preliminary data to guide future large scale research on the critical, yet understudied, psychosocial issue of body image functioning for head and neck cancer patients. Information obtained from this study can specifically be used to facilitate the development of appropriate disease-specific body image instruments and to determine the need for body image focused psychosocial interventions to enhance quality of life and the survivorship experience for these patients.

Primary Aims

1. To characterize the nature and extent of body image concerns in surgically treated patients with head and neck cancer and determine preferences for psychosocial intervention.
2. To compare body image and quality of life outcomes for patients at different time points relative to initiation of treatment. Specific time points of interest are pre-treatment, within one year of initial surgical treatment, and greater than 1 year following initial surgical treatment.

Secondary Aim

1. To compare body image and quality of life outcomes for patients with oral cavity, cutaneous, and midface cancers.
.
Study Status Information
Study Activation / Registration Date:12/08/2008
IRB Review and Approval Date:03/19/2008
Study Type:Behavioral
Recruitment Status:Closed
Projected Accrual:N/A
.
Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) 18 years of age or older

2) able to provide written informed consent to participate

3) diagnosis of oral cavity, cutaneous or other midface cancer involving the head and neck region

4) treatment plan includes surgical intervention

5) English speaking

Exclusion Criteria:1) significant preexisting facial disfigurement from a previous trauma or congenital defect

2) diagnosis of a serious mental illness involving formal thought disorder (e.g., schizophrenia) documented in medical record

3) cognitive impairment (e.g., dementia, delirium)

.
Links
Registration Number: NCT00824174
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
.
Results


Return to Clinical Trials at M.D. Anderson Cancer Center