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Trial Title:
What is the Optimal Training Model for Cervical Awareness?
NCT ID:
NCT06562595
Condition:
HPV Infection
Cervical Cancer
Cervical Dysplasia
Conditions: Official terms:
Papillomavirus Infections
Uterine Cervical Dysplasia
Study type:
Interventional
Study phase:
N/A
Overall status:
Active, not recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
The training methods employed comprise four arms:
1. Video-based training,
2. Classical lecturing,
3. Brochure,
4. Voice recording (Radio broadcast).
Primary purpose:
Health Services Research
Masking:
Single (Participant)
Masking description:
The participant will be randomly assigned to one of the four experimental groups by a
computerised randomisation software.
Intervention:
Intervention type:
Behavioral
Intervention name:
Education Intervention
Description:
Training will be provided to the participants, with the objective of determining the most
accurate training method on HPV and cervical awareness.
Arm group label:
Brochure
Arm group label:
Classical Lectures
Arm group label:
Sound Recording (Radio Broadcast)
Arm group label:
Video Assisted
Summary:
Cervical cancer represents the fourth most prevalent malignant disease and the fourth
leading cause of mortality among women on a global scale. Despite screening and
preventive vaccination efforts, cervical cancer remains a significant cause of morbidity
and mortality in low- and middle-income countries.
Detailed description:
A number of studies have been conducted with the aim of raising awareness about HPV and
cervical cancer. However, there is currently no evidence-based consensus on the most
effective method of education. The objective of this study is to identify the optimal
training method by conducting a randomised controlled trial among healthcare
professionals. The training methods under consideration are as follows: 1) Video-based
training, 2) Classical lecture training, 3) Brochure, 4) Audio recording (Radio
broadcast).
Prior to the commencement of the designated training methods, participants will be
required to complete a web-based pre-test. Subsequent to this, the system will
automatically assign each participant to a training intervention. Upon completion of the
training programme, participants will be required to undertake a second test, the results
of which will inform the selection of the most effective training method.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
Being over 18 and under 40
- Female doctors, female nurses and female health technicians
- Working in our hospital
- Having sufficient mental capacity
- Not having a visual or auditory disability
- Volunteering to participate in the study
Exclusion Criteria:
- Under 18 and over 40
- Not being a healthcare worker
- Not having enough mental capacity
- Having a visual or auditory disability
- Patients who did not volunteer to participate in the study
Gender:
Female
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
Izmir City Hospital
Address:
City:
İzmir
Country:
Turkey
Start date:
August 15, 2024
Completion date:
September 30, 2024
Lead sponsor:
Agency:
Izmir City Hospital
Agency class:
Other
Source:
Izmir City Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06562595
