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Clinical Trials/NCT06684067
NCT06684067
Completed
N/A

A Prospective Randomized Controlled Trial to Evaluate the Effect of Patient Navigation on Colonoscopy Screening Rate for Colorectal Cancer (CRC) in University Malaya Medical Centre (UMMC)

University of Malaya1 site in 1 country52 target enrollmentFebruary 3, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Colorectal Cancer Screening
Sponsor
University of Malaya
Enrollment
52
Locations
1
Primary Endpoint
Colonoscopy completion rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this randomized controlled trial is to evaluate the effectiveness of patient navigation on colonoscopy completion rates in a population screened for colorectal cancer. The main question[s] it aims to answer are:

Are colonoscopy completion rates in colorectal cancer screening increased in navigated (intervention arm) compared with non-navigated (control arm) participants?

Is mental well-being, as measured by HADs and GHQ12 scores, better in the intervention arm compared with the control arm?

Participants in the intervention arm will receive:

  • standard clinic instructions for the colonoscopy
  • phone calls from the patient navigator to discuss the purpose, preparation, and additional information regarding the colonoscopy procedure
  • a webpage QR code consist of information on visual image on colonoscopy preparation and procedures, layout and map guidance to navigate in the hospital
  • a direct line for phone calls to patient navigators for further guidance on overcoming barriers

Participants in the control arm will only receive:

  • standard clinic instructions for the colonoscopy
  • one phone call from the patient navigator to discuss the colonoscopy procedure
Registry
clinicaltrials.gov
Start Date
February 3, 2020
End Date
March 31, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Average risk for CRC
  • More than 50 years of age
  • Capacity for informed consent
  • IFOBT positive

Exclusion Criteria

  • Moderate or high risk CRC
  • Previous CRC screening
  • Symptomatic

Outcomes

Primary Outcomes

Colonoscopy completion rate

Time Frame: 90 days

The numerator in both arms comprises participants who successfully attended and underwent colonoscopy within 90 days of recruitment. The denominator in both arms comprises all participants randomized to that arm. Colonoscopy completion rate was defined as the percentage of participants who completed colonoscopy within 90 days of randomization.

Secondary Outcomes

  • Mental health - anxiety and depression(90 days)
  • Mental health - General psychological distress(90 days)

Study Sites (1)

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