Patient Reported Outcomes in the Medical Oncology Setting (iPROMOS)

Not Applicable

Completed

• Conditions: cancer; Cancer - Any cancer; Public Health - Health service research

• Registration Number: ACTRN12618000398202
• Lead Sponsor: atasha Roberts

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-03-20
• Study Completion: 2019-06-19
• Last Update Posted: 20 November 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 461

Inclusion Criteria

1. patients attending for medical review in randomized medical oncology outpatient clinics
2. Staff caring for the patients attending the randomized medical oncology outpatient clinics

Exclusion Criteria

1. Difficulty completing or understanding the PRO forms including significant cognitive impairment, visual difficulties or non-English speaking background
2. Staff that are not willing to participate

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Successful implementation as defined as, 1) PRO reports made available in the medical record to staff as per protocol in 90% of patient encounters, 2) 75% of clinicians responding to PRO data, and 3) of those, 50% of responses to PRO data noted in the medical record<br>This data will be assessed from metrics in the REDCap database, from Case Report Forms completed by clinicians and review of medical records[ 90 days post intervention commencement]

Secondary Outcome Measures

Name	Time	Method
Objective outcome measures to be assessed by review of medical records including hospital admissions and emergency room presentations. [ Day 90 post intervention commencement];Survival as assessed by medical record review[ 90 days and 12 months post commencement of intervention.<br><br>]