CClinicalTrials.gg
Status unknownNCT00020553Updated Sep 20, 2013

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

An interventional study of psychosocial assessment and care in Psychosocial Effects of Cancer and Its Treatment, sponsored by Inflexxion, Inc.. Status unknown at 5 sites in United States. Per ClinicalTrials.gov, last updated 2013-09-20.

Sponsored by Inflexxion, Inc. · Not applicable and Interventional

The sponsor has not verified this record recently (last verified Oct 2006), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Sex
All
01

Study 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.

Read the detailed 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.

02

Conditions studied

  • Psychosocial Effects of Cancer and Its Treatment

Keywords

  • psychosocial effects of cancer and its treatment
03

In context

Lead sponsor

Inflexxion, Inc. is the lead sponsor of 9 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility 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

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

05

Study design

Phase
Not applicable

Interventions

  • Procedurepsychosocial assessment and care
06

Study locations

5 sites
  • Maine Center for Cancer Medicine and Blood Disorders
    Scarborough, Maine 04074, United States
  • Inflexxion
    Newton, Massachusetts 02464-1594, United States
  • Albert Einstein Comprehensive Cancer Center
    Bronx, New York 10461, United States
  • Buddy Kemp Caring House
    Charlotte, North Carolina 28207, United States
  • Baylor University Medical Center
    Dallas, Texas 75246, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00020553
Lead sponsor
Inflexxion, Inc.
Collaborators
National Cancer Institute (NCI)
First posted
Feb 16, 2004
Start date
Aug 2000
Last update
Sep 20, 2013

Study contacts

Jonas I. Bromberg
study chair · Inflexxion, Inc.
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2006. You cannot join it, but the record below documents what was studied.

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