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Clinical Trials/NCT03899441
NCT03899441
Completed
N/A

Does Multimedia Perioperative Teaching Improve Patient Experience in the Treatment of Endometrial Cancer

UNC Lineberger Comprehensive Cancer Center1 site in 1 country87 target enrollmentOctober 1, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Endometrium Cancer
Sponsor
UNC Lineberger Comprehensive Cancer Center
Enrollment
87
Locations
1
Primary Endpoint
Patient satisfaction
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This is an interventional trial to introduce two short animated videos into preoperative counseling/consent and to compare patient comprehension and satisfaction with a multimedia approach compared to standard of care currently. The investigators anticipate that patients will retain more information about their surgery and peri-operative care and will be more satisfied with a multimedia approach.

Detailed Description

The investigators plan a pilot study where patients will be randomized to receiving standard consent and teaching prior to their planned surgery for endometrial cancer or standard consent and multimedia video aid with targeted teaching. This video will be an adjunct to the standard consent process and supplement the pre and post-operative teaching that is currently not formalized. The primary outcome is patient satisfaction. The secondary outcomes include patient understanding and physician satisfaction. The investigators hypothesize that patients will be more satisfied when their consent for surgery is done in conjunction with this multimedia aid.

Registry
clinicaltrials.gov
Start Date
October 1, 2018
End Date
April 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • English-speaking
  • Has diagnosis of endometrial cancer
  • Planned minimally invasive surgical treatment with hysterectomy and sentinel lymph node biopsy

Exclusion Criteria

  • Non-English speaking

Outcomes

Primary Outcomes

Patient satisfaction

Time Frame: 1 day (assessed at first visit)

Patient satisfaction with the clinic visit (either new patient visit where they are consented for surgery or a pre-operative visit). Patient satisfaction will be measured using two survey tools: a single question to assess global satisfaction with the clinic visit (on a scale from 1-10) and an 8 question validated satisfaction survey (Client Satisfaction Questionnaire-8 or CSQ-8). Patient satisfaction will be compared between the control and intervention groups. For the single question satisfaction question, answers are on a scale from 1-10, the higher numbers indicating higher satisfaction. The CSQ8 survey contains 8 questions that all have answers ranging from 1 to 4, with higher numbers indicating higher satisfaction.

Secondary Outcomes

  • Patient comprehension(6-8 weeks (assessed at 3 time points - first clinic visit, inpatient at time of surgery, and at follow-up visit 4-6 weeks after surgery))
  • Physician satisfaction(1 day (assessed at first visit))
  • Visit length(1 day (assessed during first visit))

Study Sites (1)

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