Clinical Trials Logo
  1. Home
  2. Other
  3. NCT00020553
  4. Details
NCT00020553 Clinical Trial

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

Psychosocial Effects of Cancer and Its Treatment Clinical Trial

Official title:
We Can Cope: Family Support When A Parent Has Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00020553
Other study ID # CDR0000068602
Secondary ID INFLEXXION-00008
Status Active, not recruiting
Phase N/A
First received July 11, 2001
Last updated September 19, 2013
Start date August 2000

Study information
Verified date October 2006
Source National Cancer Institute (NCI)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

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.

Description:

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.

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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility 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

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

PRIOR CONCURRENT THERAPY: Not specified

Study Design

N/A

Related Conditions & MeSH terms

  • Psychosocial Effects of Cancer and Its Treatment

Intervention

Procedure:
• psychosocial assessment and care

Locations
Country Name City State
United States Albert Einstein Comprehensive Cancer Center Bronx New York
United States Buddy Kemp Caring House Charlotte North Carolina
United States Baylor University Medical Center Dallas Texas
United States Inflexxion Newton Massachusetts
United States Maine Center for Cancer Medicine and Blood Disorders Scarborough Maine

Sponsors (2)
Lead Sponsor Collaborator
Inflexxion, Inc. National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

See also
  Status Clinical Trial Phase
Completed NCT01434290 - Radiation Therapy in Treating Patients With Prostate Cancer Phase 2
Completed NCT00830635 - Multimedia Educational Program for Patients With Early-Stage Prostate Cancer or Breast Cancer N/A
Completed NCT00951626 - A Standardized Nursing Intervention Protocol for HCT Patients N/A
Completed NCT00466830 - Psychological and Social Factors That May Increase the Risk of Developing Chronic Pain After Surgery in Women With Breast Cancer N/A
Completed NCT01846520 - Family Caregiver Palliative Care Intervention in Supporting Caregivers of Patients With Stage II-IV Gastrointestinal, Gynecologic, Urologic and Lung Cancers N/A
Withdrawn NCT00397501 - BBBD Followed By Methotrexate and Carboplatin With or Without Trastuzumab in Treating Women With Breast Cancer That Has Spread to the Brain Phase 1/Phase 2
Completed NCT01417507 - Natural History of Brain Function, Quality of Life, and Seizure Control in Patients With Brain Tumor Who Have Undergone Surgery N/A
Completed NCT01217424 - Reflexology or Aromatherapy Massage in Relieving Symptoms in Patients With Cancer N/A
Completed NCT00956475 - Quality of Life in Younger Leukemia and Lymphoma Survivors Phase 1
Withdrawn NCT00873600 - Outpatient Health Care Program for Older Patients Receiving Chemotherapy for Newly Diagnosed Breast Cancer or Colon Cancer N/A
Completed NCT00932997 - Survivorship Booklets With or Without Individual Telephone Sessions in Increasing Knowledge About the Impact of Breast Cancer in African American and Latina Breast Cancer Survivors N/A
Completed NCT00400699 - Radiation Therapy Outreach Program for Minority or Low-Income Patients With Newly Diagnosed Cancer N/A
Completed NCT00915889 - Psychosocial Support for African-American, Latina-American, or European-American Cervical Cancer Survivors N/A
Completed NCT00363909 - Citalopram in Treating Postmenopausal Women With Hot Flashes Phase 3
Completed NCT00410579 - Patient-Reported Outcomes in Long-Term Survivors of Colon and Rectal Cancers N/A
Completed NCT00713505 - Educational and Skills Training Program for Parents of Childhood Cancer Survivors Who Have Neurobehavioral Dysfunction N/A
Withdrawn NCT00770419 - Perceptions of Burden in Patients With Late-Stage Cancer and Their Caregivers N/A
Recruiting NCT00503646 - Communication and Intimacy-Enhancing Therapy for Men With Early Stage Prostate Cancer and Their Partners N/A
Completed NCT00755313 - Effects of Chemotherapy on the Brain in Women With Newly Diagnosed Early-Stage Breast Cancer N/A
Completed NCT00372840 - Printed Education Materials in Patients Who Are Finishing Treatment for Stage I, Stage II, or Stage IIIA Breast Cancer, Colorectal Cancer, Prostate Cancer, or Chest Cancer N/A