- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00425139
Evaluation of a Video Game for Adolescents and Young Adults With Cancer
Multi-site Evaluation of a Video Game for Adolescents and Young Adults With Cancer
Panoramica dello studio
Descrizione dettagliata
POPULATION: Approximately 340 patients will be enrolled in this study. Patients will be 13 to 29 years of age with any cancer (original diagnosis or relapse), currently receiving treatment and expected to be on treatment for at least 4 - 6 months following Baseline assessment, and able to communicate effectively in English, Spanish, or French. Approximately 170 patients will be enrolled in each of the two treatment groups. Each group will receive either the "Re-Mission" video game and a popular interactive video game, or just the popular interactive video game.
DESIGN: This is a multi-center, randomized trial, with patients randomized to one of two groups. One group (50% of patients) will receive the active intervention, which is the psycho-educational video game module called Re-Mission and a popular video game (hereafter "RE-MISSION") and another group (50 % of patients) will be in a game control group and receive a popular video game only (hereafter "GAME CONTROL. The games in the RE-MISSION and GAME CONTROL groups are delivered on identical mini, personal computers (hereafter "Mini-PC").
INTERVENTION: Each patient in the RE-MISSION group will be asked to play "Re-Mission" along with the popular video game for at least one hour a week for a period of ten to fourteen weeks. "Re-Mission" presents a 3-D environment in which the player can manipulate a humanoid character inside the virtual body of a patient with cancer. Game-play consists of guiding the character to destroy cancer cells and other "enemies" in the body (e.g., bacteria) while avoiding injury or weakness. During the process of playing the game and guiding the character through a series of missions, the player learns about chemotherapy and other medical treatments, health-promoting self-care behaviors, infections, and pain management. In addition, the game has also been designed to facilitate the patient's ability to share knowledge and concerns with others.
DURATION OF STUDY: 9 -12 months
Tipo di studio
Iscrizione
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Victoria
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Parkville, Victoria, Australia, 03052
- Royal Children's Hospital
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Alberta
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Calgary, Alberta, Canada, T2T 5C7
- Calgary Alberta Children's Hospital
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Ontario
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Hamilton, Ontario, Canada, L8N 3Z5
- McMaster University
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Ottawa, Ontario, Canada, K1H 8LI
- Children's Hospital of Eastern Ontario
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Quebec
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Montreal, Quebec, Canada, H3H 1P3
- McGill Univ Health Ctr - Montreal Children's Hospital
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Montreal, Quebec, Canada, H3T 1C5
- Hôpital Ste-Justine
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Ste-Foy, Quebec, Canada, G1V 4G2
- Centre Hospitalier Universitaire de Quebec
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California
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Duarte, California, Stati Uniti, 91010
- City of Hope National Medical Center
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Los Angeles, California, Stati Uniti, 90027
- Los Angeles Children's Center for Cancer and Blood Disease
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Orange, California, Stati Uniti, 92868
- Children's Hospital of Orange County
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Palo Alto, California, Stati Uniti, 94304
- Lucile Packard Children's Hospital at Stanford
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Florida
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Fort Myers, Florida, Stati Uniti, 33908
- Children's Hospital of SW Florida / Lee Memorial Health System
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Jacksonville, Florida, Stati Uniti, 32207
- Nemours Children's Clinic-Jacksonville
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St. Petersburg, Florida, Stati Uniti, 33701
- All Children's Hospital
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Tampa, Florida, Stati Uniti, 33607
- St. Joseph's Children's Hospital of Tampa
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Hawaii
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Honolulu, Hawaii, Stati Uniti, 96826
- Kapiolani Medical Center
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Louisiana
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New Orleans, Louisiana, Stati Uniti, 70118
- LSU Children's Hospital of New Orleans
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Massachusetts
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Boston, Massachusetts, Stati Uniti, 02115
- Dana-Farber Cancer Institute and Children's Hospital
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Michigan
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Grand Rapids, Michigan, Stati Uniti, 49503
- DeVos Children's Hospital
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Grosse Pointe Woods, Michigan, Stati Uniti, 48236
- St John Van Elslander Cancer Center
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Minnesota
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St. Paul, Minnesota, Stati Uniti, 55404
- Children's Health Care - Minneapolis
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Missouri
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Kansas City, Missouri, Stati Uniti, 64108
- Children's Mercy Hospital
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St. Louis, Missouri, Stati Uniti, 63110
- Washington University
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New Mexico
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Albuquerque, New Mexico, Stati Uniti, 87131-0001
- Children's Hospital of New Mexico
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New York
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Rochester, New York, Stati Uniti, 14642
- Golisano Children's Hospital, University of Rochester
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Oklahoma
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Tulsa, Oklahoma, Stati Uniti, 74136
- Warren Clinic / Saint Francis Hospital
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Oregon
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Portland, Oregon, Stati Uniti, 97227
- Legacy Emanuel Children's Cancer Program
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Portland, Oregon, Stati Uniti, 97239
- Doernbecher Childrens Hospital - OHSU
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Texas
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Austin, Texas, Stati Uniti, 78701-1096
- Children's Hospital of Austin
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Corpus Christi, Texas, Stati Uniti, 78411
- Driscoll Children's Hospital
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Fort Worth, Texas, Stati Uniti, 76104
- Cook Children's Medical Center
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San Antonio, Texas, Stati Uniti, 78207
- Christus Santa Rosa Children's Hospital
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Virginia
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Norfolk, Virginia, Stati Uniti, 23507
- Children's Hospital of The King's Daughters
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Washington
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Spokane, Washington, Stati Uniti, 99204
- Deaconess Medical Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Male or female patient 13 to 29 years of age with a cancer diagnosis.
- Patient who is currently receiving treatment and is expected to remain on treatment for at least 4 - 6 months.
Exclusion Criteria:
- Patient who has a history of seizures due to photosensitivity.
- Patient who has been determined by the investigator to be incapable of following the study schedule or study directions for any reason.
- Patient who can not communicate effectively with study personnel in English, Spanish, or French.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
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Qualità della vita
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Aderenza
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Autoefficacia
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Pamela M Kato, HopeLab Foundation
Pubblicazioni e link utili
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Altri numeri di identificazione dello studio
- HL-04-001
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
prodotto fabbricato ed esportato dagli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .