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Preoperative Patient Education Via Animated Videos to Improve Patient Satisfaction and Reduce Complications in Head and Neck Surgery

J

Jewish General Hospital

Status

Completed

Conditions

Surgery
Patient Satisfaction

Treatments

Other: usual standard of care
Other: Precare

Study type

Interventional

Funder types

Other

Identifiers

NCT04048538
Precare

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Treatment Arm
Experimental group
Description:
Individuals who will receive access to the animated multimedia platform prior to their surgical procedure.
Treatment:
Other: Precare
Control Arm
Active Comparator group
Description:
Individuals who will not receive access to the animated patient platform, and instead will receive the usual standard of care.
Treatment:
Other: usual standard of care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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