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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06388473
Other study ID # NMRR-20-2188-56086 IIR
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 14, 2021
Est. completion date June 6, 2021

Study information

Verified date April 2024
Source University of Malaya
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine how to successfully implement ScreenMen in the primary care setting. ScreenMen is a mobile web-based app that has been developed to increase the uptake of screening in men. ScreenMen undertook a vigorous and systematic approach in its development. It was developed based on theories, evidence and needs of men. ScreenMen particularly target men in the age group of 20 to 50 years as this group of men usually do not attend any health screening. This research is necessary because ScreenMen has yet to be implemented in the primary care setting. The study will last about five months and your participation will be about five months.


Recruitment information / eligibility

Status Completed
Enrollment 101
Est. completion date June 6, 2021
Est. primary completion date June 6, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Healthcare providers that were involved in the clinic health screening program. 2. Patients who were aged 18 years and above were eligible to participate. Exclusion Criteria: 1. Temporary healthcare providers (working in the clinic less than six months during the study period) and those who were away on leave. 2. Patients who did not understand Bahasa Malaysia, English or Mandarin, cognitively impaired, had an active psychiatric illness or were too ill.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Tailored implementation intervention
The tailored implementation intervention comprised of six implementation strategies: 1) Involve executive boards, 2) Mandate change, 3) Provide education and training, 4) Identify and prepare champions, 5) The use of information and communication technology and 6) Audit and provide feedback.

Locations

Country Name City State
Malaysia Klinik Kesihatan Cheras Baru Kuala Lumpur

Sponsors (1)

Lead Sponsor Collaborator
University of Malaya

Country where clinical trial is conducted

Malaysia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reach Number of healthcare providers who attended the workshop / Number of healthcare providers who were invited to the workshop. Beginning of intervention
Primary Reach The number of patients who accessed ScreenMen. Through study completion, 5 months.
Primary Adoption of ScreenMen using qualitative methods Factors affecting the participation of healthcare providers in adopting ScreenMen in daily practice using qualitative interviews. 5 months into study
Primary Implementation of ScreenMen using qualitative methods Factors affecting the implementation of ScreenMen daily practice using qualitative interviews. 5 months into study
Primary Maintenance of ScreenMen using qualitative methods Intention to implement ScreenMen and factors influencing the decision using qualitative methods. 5 months into study
Secondary Impact of COVID-19 on the clinic using qualitative methods The clinic situation during the COVID-19 pandemic and how it affected daily practice using qualitative methods. 5 months into study
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