Evaluation of the Use of Multimedia to Enhance Patient and Family Understanding
18. april 2012 opdateret af: Dr. David Fleiszer, McGill University Health Centre/Research Institute of the McGill University Health Centre
This study will investigate the potential impact of arts-informed, technology-based patient education material, and specifically, the role of multimedia imagery on patient comprehension, perceived satisfaction, anxiety levels, and informed decision-making.
Studieoversigt
Status
Ukendt
Intervention / Behandling
Detaljeret beskrivelse
Based on an inter-professional approach to support a new role in patient care, this research addresses both literacy and health literacy issues within the context of current challenges to healthcare delivery and associated fragmentation in continuity of care.
Patient education is a key component in the delivery of comprehensive care and it is the potential for on-line patient education that provides the basis for research.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
60
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Quebec
-
Montreal, Quebec, Canada, H3A 1A1
- Royal Victoria Hospital, Cedars Breast Clinic
-
Montreal, Quebec, Canada, H3H 2R9
- Myrna Cabaluna, Manager, MUHC Education Portfolio
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
The following inclusion criteria will be used: Participants must be:
- Newly diagnosed breast cancer patients
- A minimum age of 18 years or older
- Able to read and write in English and/or French
Have a confirmed diagnosis of any of the following:
- Infiltrating ductal carcinoma
- Ductal carcinoma in situ (Grade III)
- Lobular carcinoma in situ (Grade III)
- Infiltrating lobular carcinoma
- Have access to, and the ability to use, a computer
Exclusion Criteria:
The following criteria will be reasons for exclusion from the study:
- The participant has a serious psychiatric or cognitive impairment that would prevent the patient from completing the study requirements.
- The participant has a previous history of breast cancer
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Placebo komparator: No Media
Sixty participants will be randomized into one of two cohorts: 1.
No media 2. Yes media
|
This group will not be exposed to multimedia
|
|
Eksperimentel: Yes Media Newly Diagnosed Breast Cancer Pts
Sixty participants will be randomized into one of two cohorts: 1.
No media 2. Yes media
|
This group of patients will be exposed to multimedia
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Concept Grid
Tidsramme: 1 year
|
A likert scale measuring the comprehension and retention of key concepts in the research study.
|
1 year
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
DCS Conflict Scale
Tidsramme: 1 year
|
Traditional Decision Conflict Scale - The decisional conflict scale measures personal perceptions of: a) uncertainty in choosing options; b) modifiable factors contributing to uncertainty such as feeling uninformed, unclear about personal values and unsupported in decision making; and c) effective decision making such as feeling the choice is informed, values-based, likely to be implemented and expressing satisfaction.
|
1 year
|
|
Anxiety Scale - A.S. Zigmond and R.P. Snaith
Tidsramme: 1 year
|
A self-assessment scale that has been developed and found to be a reliable instrument for detecting states of depression and anxiety in the setting of a hospital medical outpatient clinic.
This questionnaire is designed to help the doctor know how you feel.
|
1 year
|
|
The Hospital Anxiety and Depression (HAD) Scale
Tidsramme: 1 year
|
The Hospital Anxiety and Depression (HAD) rating scale is a commonly used questionnaire.
It is a screening questionnaire for psychiatric disorders.
|
1 year
|
|
Interactive Patient Education Oncology Module
Tidsramme: 1 year
|
We would like to know if the module helped the patient understand their disease and their available treatment options.
It is a questionnaire to obtain feedback on its overall design.
|
1 year
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: David Fleiszer, M.D.C.M., F.R.C.S (C)., McGill University Health Centre/Research Institute of the McGill University Health Centre
- Studieleder: Nancy Posel, N. DIA, M.Ed, PhD, McGill University
- Studiestol: Dianne Bateman, PhD, McGill University
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- del Carmen MG, Joffe S. Informed consent for medical treatment and research: a review. Oncologist. 2005 Sep;10(8):636-41. doi: 10.1634/theoncologist.10-8-636.
- Etchells E, Sharpe G, Walsh P, Williams JR, Singer PA. Bioethics for clinicians: 1. Consent. CMAJ. 1996 Jul 15;155(2):177-80.
- Beamond BM, Beischer AD, Brodsky JW, Leslie H. Improvement in surgical consent with a preoperative multimedia patient education tool: a pilot study. Foot Ankle Int. 2009 Jul;30(7):619-26. doi: 10.3113/FAI.2009.0619. Erratum In: Foot Ankle Int. 2009 Sep;30(9):vi.
- Patel V, Aggarwal R, Kinross J, Taylor D, Davies R, Darzi A. Improving informed consent of surgical patients using a multimedia-based program?: results of a prospective randomized multicenter study of patients before cholecystectomy. Ann Surg. 2009 Mar;249(3):546-7; author reply 547-8. doi: 10.1097/SLA.0b013e31819abeb1. No abstract available.
- Eggers C, Obliers R, Koerfer A, Thomas W, Koehle K, Hoelscher AH, Bollschweiler E. A multimedia tool for the informed consent of patients prior to gastric banding. Obesity (Silver Spring). 2007 Nov;15(11):2866-73. doi: 10.1038/oby.2007.340.
- Ryhanen AM, Siekkinen M, Rankinen S, Korvenranta H, Leino-Kilpi H. The effects of Internet or interactive computer-based patient education in the field of breast cancer: a systematic literature review. Patient Educ Couns. 2010 Apr;79(1):5-13. doi: 10.1016/j.pec.2009.08.005. Epub 2009 Sep 9.
- Sandberg EH, Sharma R, Wiklund R, Sandberg WS. Clinicians consistently exceed a typical person's short-term memory during preoperative teaching. Anesth Analg. 2008 Sep;107(3):972-8. doi: 10.1213/ane.0b013e31817eea85.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2010
Primær færdiggørelse (Forventet)
1. december 2012
Studieafslutning (Forventet)
1. januar 2013
Datoer for studieregistrering
Først indsendt
17. juni 2010
Først indsendt, der opfyldte QC-kriterier
28. juni 2010
Først opslået (Skøn)
29. juni 2010
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
20. april 2012
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. april 2012
Sidst verificeret
1. april 2012
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 09-269-PSY
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 .