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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04048538
Other study ID # Precare
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2019
Est. completion date January 30, 2021

Study information

Verified date October 2021
Source Jewish General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This randomized control trial will compare traditional patient education methods (pamphlets, clinical visits) to the implementation of an innovated patient education platform. The purpose of the project is to determine whether the use of this animation based patient education platform prior to undergoing surgery will lead to improved patient satisfaction and quality of life.


Description:

Hypothesis/Study question: Does the implementation of an animation based patient education platform prior to undergoing surgery lead to improved patient satisfaction and quality of life? Study objectives: Help address patient gaps in understanding, reduce learning barriers in order for patients to make informed decisions, improve behaviors, and better partner with their health providers to attain optimal health outcomes Methodology / Study design: Patients will receive access to the patient education platform during the clinical visit in which they receive their diagnosis, and will be asked if they wish to enroll in the study consisting of completing questionnaires before and after their surgical procedure. Questions will inquire on levels of anxiety, patient satisfaction, knowledge retention, and platform feedback.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 30, 2021
Est. primary completion date December 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Individuals having any of the following surgical procedure at the Jewish General Hospital over the next 12 months: head and neck cancer resection with or without reconstruction, excision of parotid lesion, thyroidectomy, parathyroidectomy, laryngectomy, or trans-oral robotic resection. Exclusion Criteria: - Individuals who are undergoing a surgical procedure not included in the ones listed above, or those who are having revision surgery or have previously had surgery in the otolaryngology, head and neck surgery department.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Precare
an innovative patient education platform using animated videos created by using up-to-date evidence-based informaiton
usual standard of care
individuals will receive treatment as per the usual standard of care

Locations

Country Name City State
Canada Jewish General Hospital Montreal Quebec

Sponsors (1)

Lead Sponsor Collaborator
Jewish General Hospital

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Satisfaction analyzed using patient questionnaire responses 1 month post-operative
Secondary Post-operative complication rate analyzed using hospital data 1 month post-operative
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