- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00020553
Video Support Program For Families With a Parent Newly Diagnosed With Cancer
We Can Cope: Family Support When A Parent Has Cancer
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.
Studieoversigt
Status
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
Maine
-
Scarborough, Maine, Forenede Stater, 04074
- Maine Center for Cancer Medicine and Blood Disorders
-
-
Massachusetts
-
Newton, Massachusetts, Forenede Stater, 02464-1594
- Inflexxion
-
-
New York
-
Bronx, New York, Forenede Stater, 10461
- Albert Einstein Comprehensive Cancer Center
-
-
North Carolina
-
Charlotte, North Carolina, Forenede Stater, 28207
- Buddy Kemp Caring House
-
-
Texas
-
Dallas, Texas, Forenede Stater, 75246
- Baylor University Medical Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Studiestol: Jonas I. Bromberg, Inflexxion, Inc.
Datoer for undersøgelser
Studer store datoer
Studiestart
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- CDR0000068602
- INFLEXXION-000080
- ITS-000080
- NCI-V01-1659
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med psykosocial vurdering og omsorg
-
Dana-Farber Cancer InstituteAfsluttetKræft | Kemoterapi-induceret perifer neuropatiForenede Stater
-
Medipol UniversityAfsluttetCAD test; børns vision; Farvevurdering; Farvesyn; KalkunKalkun
-
VA Office of Research and DevelopmentRekrutteringSlag | BalanceunderskudForenede Stater
-
Indiana UniversityIndiana University HealthAfsluttetMetastatisk kræft | Avanceret kræftForenede Stater
-
Indiana UniversityIndiana University Health; Regenstrief Institute, Inc.AfsluttetDepression | PTSD | Angst | Meddelelse | TilfredshedForenede Stater
-
Medical University of South CarolinaNational Institute for Biomedical Imaging and Bioengineering (NIBIB)AfsluttetTræthed | SarcoidoseForenede Stater
-
University of CincinnatiNational Institute of Nursing Research (NINR)RekrutteringSlag | FamilieplejereForenede Stater
-
Jessa HospitalAfsluttetAr | Minimalt invasiv hjertekirurgiBelgien
-
SAE OrthopedicsIkke rekrutterer endnu
-
University of North Carolina, Chapel HillViiV HealthcareAfsluttet