- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01645904
A Social Media Approach to Improve Genetic Risk Communication Phase I
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
If you agree to take part in this study, you will be assigned to 1 of 3 groups based on when you joined the study.
Group 1:
If you are assigned to Group 1, you will take part in a focus group where you will be asked what you would want in a web-based program designed to improve the communication of health and health history information among family members affected by Lynch syndrome. You will also fill out a questionnaire with questions about your demographics (age, race, marital status) and your medical history. This visit should take about 1 hour to complete.
Group 2:
If you are assigned to Group 2, you will come to the Behavioral Research and Treatment Center (BRTC) at MD Anderson to use the initial version of the My Family Garden website. My Family Garden is designed to teach new ways of communicating about Lynch Syndrome and about other issues related to the disease (such as risks associated with the disease, etc.). You will be instructed on how to use the program by the study staff. After you use the website, you will have an interview where you will provide feedback on your session. You will be asked questions about your feelings about the website and about any possible improvements that could be made to the website. You will also fill out a questionnaire called the Website Analysis and MeasureMent Inventory (WAMMI) which is designed help rate websites. You will also fill out the demographics questionnaire described above.
You will be given the option of completing the WAMMI and demographics questionnaire at the BRTC after your session or at your home. If you choose to complete them at home, you will be provided with a self-addressed, postage-paid envelope so you can mail the questionnaires back to the study staff.
This visit should take about 90 minutes to complete.
Group 3:
If you are assigned to Group 3, you will use the final version of the My Family Garden website. This final version will include changes from the web designers after feedback has been given from the previous groups in this study.
After you use the website, you will have an interview where you will provide feedback on your session. You will be asked questions about your feelings about the website and about any possible improvements that could be made to the website. You will also fill out the WAMMI questionnaire and demographics questionnaire described above.
You will be given the option of coming to the BRTC at MD Anderson to use the My Family Garden computer program or using the program from your home. If you choose to use My Family Garden from your home, you will be given a secure, password-protected hyperlink via e-mail to access the program. You will be instructed on how to use the program by the study staff either in person or over the phone. If you use the program from your home, the study staff will give the interview over the phone. If you complete the questionnaire at your home, you will be provided with a self-addressed, postage-paid envelope so you can mail it back to the study staff.
Whether it is completed at MD Anderson or at home, this visit should last about 90 minutes.
Audiotapes:
All focus groups and interviews will be audiotaped. The audiotapes collected during the course of this study will be stored in locked file cabinets in a locked office and will be destroyed after 5 years.
Length of Study Participation:
Your participation in this study will be over after you have completed the study procedures described above.
This is an investigational study.
Up to 49 participants will be enrolled in this study. All participants will be enrolled at MD Anderson.
Tipo di studio
Iscrizione (Anticipato)
Contatti e Sedi
Luoghi di studio
-
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Texas
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Houston, Texas, Stati Uniti, 77030
- University of Texas MD Anderson Cancer Center
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
- At least 18 years of age
- Able to read and speak english
- Completion of genetic counseling and testing for a Lynch syndrome mutation
- Persons with positive (i.e., carrier of Lynch syndrome MMR mutation) as well as indeterminate test results
Exclusion Criteria:
1) None
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Modelli osservazionali: Basato sulla famiglia
- Prospettive temporali: Prospettiva
Coorti e interventi
Gruppo / Coorte |
Intervento / Trattamento |
---|---|
Group 1
Patients participate in audiotaped focus group regarding web-based program, and fill out demographics questionnaire.
|
Participation in a focus group regarding web-based program designed to improve communication of health and health history information among family members affected by Lynch syndrome.
Complete questions about demographics (age, race, marital status) and medical history.
This visit should take about 1 hour to complete.
Altri nomi:
|
Group 2
Patients come to Behavioral Research and Treatment Center (BRTC) at MD Anderson to use initial version of My Family Garden website.
Completion of Website Analysis and MeasureMent Inventory (WAMMI), and demographics questionnaires.
|
Complete questions about demographics (age, race, marital status) and medical history.
This visit should take about 1 hour to complete.
Altri nomi:
Group 2: Patients provide feedback regarding initial version of My Family Garden website. Group 3: Patients provide feedback regarding final version of My Family Garden website.
Patients complete Website Analysis and MeasureMent Inventory.
This visit should take about 90 minutes to complete.
|
Group 3
Patients use final version of My Family Garden website, and are interviewed which will be audiotaped.
Completion of Website Analysis and MeasureMent Inventory (WAMMI), questionnaire and demographics questionnaire.
|
Complete questions about demographics (age, race, marital status) and medical history.
This visit should take about 1 hour to complete.
Altri nomi:
Group 2: Patients provide feedback regarding initial version of My Family Garden website. Group 3: Patients provide feedback regarding final version of My Family Garden website.
Patients complete Website Analysis and MeasureMent Inventory.
This visit should take about 90 minutes to complete.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Evaluation of Internet-Based Program Among Lynch Syndrome Family Members
Lasso di tempo: 1 day
|
Quantitative analysis include descriptive statistics summarizing participants' demographic and clinical characteristics.
Descriptive statistics calculated for each subscale of Website Analysis and MeasureMent Inventory (WAMMI) and for overall measure.
Focus groups and interviews transcribed, coded and analyzed.
Responses sorted into categorical and conceptual groups, field notes taken during user testing also used to aid in interpretation of interview data.
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1 day
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Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Susan Peterson, MPH, PhD, M.D. Anderson Cancer Center
Pubblicazioni e link utili
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
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 (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 2012-0418
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 .
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