Ignite Creation Date:
2024-05-06 @ 7:55 PM
Last Modification Date:
2024-10-26 @ 3:16 PM
Study NCT ID:
NCT06181344
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-01-03
First Post:
2023-12-12
Brief Title:
Implementation and Evaluation of a Fear of Cancer Recurrence Screening Referral and Management Program
Sponsor:
The University of Hong Kong
Organization:
The University of Hong Kong
Study Overview
Official Title:
Implementation and Evaluation of a Fear of Cancer Recurrence Screening Referral and Management Program for Chinese Cancer Survivors a Stepped Wedge and Cluster Randomized Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2023-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to evaluate the process and outcomes of an implementation program designed to implement fear of cancer screening referral and management into routine cancer care clinics using a stepped-wedge cluster randomized controlled trial
Detailed Description:
This study aims to test if a systematic fear of cancer screening program that employs implementation strategies including training reflecting evaluating facilitating and adapting increases the proportion of eligible patients screened and referred compared to usual control with no implantation strategies used This study hypothesize that the implementation program will increase i the proportion of eligible patients screened and ii the proportion of patients with high fear of cancer referred for psychosocial support For process evaluation this study aims to use qualitative methods to assess the patients and service providers experience of the implementation program and identify contextual factors eg potential barriers and facilitators likely to influence its adoption implementation and sustainability
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None