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Video Support Program For Families With a Parent Newly Diagnosed With Cancer



Video Support Program For Families With a Parent Newly Diagnosed With Cancer

For Condition: psychosocial effects/treatment
Status: No longer recruiting
Sponsor(s): National Cancer Institute (NCI) , Inflexxion
Synopsis: RATIONALE: A videotape support program may help families improve communication and coping skills when a parent is diagnosed with cancer. PURPOSE: Randomized trial to study the effectiveness of a video support program for families who have a parent who has been newly diagnosed with cancer. This clinical trial is being conducted at the locations listed below. If you are interested in this clinical trial but unable to visit these locations, please call 1-800-848-3895, extension 226, and ask for more information about the We Can Cope study.
Details: OBJECTIVES: I. Determine if families who participate in a video support program function better as a family in the areas of communication, togetherness, and overall increased ability to cope when a parent is newly diagnosed with cancer. II. Determine if participation in this program decreases stress-related illness in the well members of the family. III. Determine the safety of this program. IV. Determine patient/family and medical provider satisfaction with this program. PROTOCOL OUTLINE: This a randomized study. Adult parent participants and spouses undergo a baseline assessment over approximately 1 hour comprising completion of a self-assessment form followed by an interview. Families are then randomized to one of two arms. Arm I: Adult parent participants receive a video support program comprising 3 videotapes (parent tape, adolescent tape, and child tape) and a parent guidebook. The parents are encouraged to screen the videotapes and decide whether to have their child and/or adolescent view the program. Arm II: Adult parent participants receive no video support material. Families may view the video program after study completion. Adult parent participants in both arms complete follow-up assessments at 6 and 12 weeks. This clinical trial is being conducted at the locations listed below. If you are interested in this clinical trial but unable to visit these locations, please call #1-800-848-3895 ext. 226 and ask for more information about the We Can Cope study. PROJECTED ACCRUAL: A total of 230 families will be accrued for this study.
Eligibility:
Study Type:
  Interventional, Educational/Counseling/Training
Minimum Age/Maximum Age: /
Genders: 
Protocol Entry Criteria: PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- - Parent with a first diagnosis of cancer within the past 5 years - No recurrence of a previously diagnosed cancer - Must have at least 1 child between the ages of 6 and 18 - Ill parent must live with child/children at least 50% of the time - No plans to move out-of-state within the next 3 months --Prior/Concurrent Therapy-- - Not specified --Patient Characteristics-- - Age: See Disease Characteristics; Any age - Performance status: Not specified - Life expectancy: Not specified - Hematopoietic: Not specified - Hepatic: Not specified - Renal: Not specified - Other: No psychotic disorder (such as schizophrenia) or a brain/psychiatric disorder due to disease/illness
Total Enrollment: 

Location and Contact Information:

Overall Study Official:
JonasBromberg,  Study Chair,  Inflexxion

Buddy Kemp Caring House
Charlotte,  North Carolina,  28207
United States
 

Albert Einstein Comprehensive Cancer Center
Bronx,  New York,  10461
United States
 

Inflexxion
Newton,  Massachusetts,  02464-1594
United States
 

Baylor University Medical Center
Dallas,  Texas,  75246
United States
 

Maine Center for Cancer Medicine and Blood Disorders
Scarborough,  Maine,  04074
United States
 


Additional Information:
Study ID Numbers:
  CDR0000068602;  NCI-V01-1659,ITS-000080
Study Start Date: August 2000
Record last reviewed: February 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00020553

Other Psychosocial Effects/treatment Studies:
1. Effectiveness of Telephone Counseling By Breast Cancer Survivors on the Well-Being of Women With Recurrent Breast Cancer

2. Group Therapy Compared With Educational Materials in Patients With Prostate Cancer

3. Stress Reduction in Older Women With Stage II, Stage III, or Stage IV Breast Cancer

4. Evaluating Patient Participation in Phase I Clinical Trials

5. Development of Strategies to Increase Enrollment in Clinical Trials for Children With Cancer

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Video Support Program For Families With a Parent Newly Diagnosed With Cancer

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