The Effect of E-health Video Towards Enhancing Cervical Cancer Screening
Primary Purpose
Cervical Cancer Screening
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
E-health Video KaSEH
Brochure
Sponsored by
About this trial
This is an interventional screening trial for Cervical Cancer Screening
Eligibility Criteria
Inclusion Criteria:
- Women who have never undergone cervical cancer screening.
Exclusion Criteria:
- Women who have been diagnosed or are cervical cancer patients
- Women who have been diagnosed with any cancer of the gynecological system such as cancer of the vulva, vagina, uterus, fallopian tubes and ovaries.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Intervention group
Control group
Arm Description
Receive the e-health video and brochure as the intervention
Receive brochure as the intervention
Outcomes
Primary Outcome Measures
Motivation level
The score of motivation level measured by means (standard deviation) using The Malay-Protection Motivation Theory scale for cervical cancer screening as measurement tool.
Practice
Measured by yes (uptake of cervical cancer screening) and no (did not perform screening).
Secondary Outcome Measures
Full Information
NCT ID
NCT05426642
First Posted
June 15, 2022
Last Updated
June 20, 2022
Sponsor
Universiti Kebangsaan Malaysia Medical Centre
1. Study Identification
Unique Protocol Identification Number
NCT05426642
Brief Title
The Effect of E-health Video Towards Enhancing Cervical Cancer Screening
Official Title
Development and Evaluation of KaSEH Video to Increase Women's Knowledge and Motivation Regarding Cervical Cancer and Its Screening.
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
October 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universiti Kebangsaan Malaysia Medical Centre
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The aim of this quasi-experimental study is to evaluate the women's motivation related to cervical cancer screening. The experiment group will receive the e-health video KaSEH and brochure as the intervention. Where as, the control group will receive brochure as the intervention. There is three phase of evaluation which are pre-intervention, intra-intervention and post-intervention. The evaluation will be assess using the self-administered questionnaire based on Protection Motivation Theory. The estimated duration of this quasi-experiment is six month.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Cancer Screening
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Receive the e-health video and brochure as the intervention
Arm Title
Control group
Arm Type
Other
Arm Description
Receive brochure as the intervention
Intervention Type
Other
Intervention Name(s)
E-health Video KaSEH
Intervention Description
The e-health video KaSEH is produce based on Protection Motivation Theory to enhance women's motivation towards cervical cancer screening.
Intervention Type
Other
Intervention Name(s)
Brochure
Intervention Description
The brochure contain the information regarding cervical cancer and its screening
Primary Outcome Measure Information:
Title
Motivation level
Description
The score of motivation level measured by means (standard deviation) using The Malay-Protection Motivation Theory scale for cervical cancer screening as measurement tool.
Time Frame
3 month
Title
Practice
Description
Measured by yes (uptake of cervical cancer screening) and no (did not perform screening).
Time Frame
3 month
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Women who have never undergone cervical cancer screening.
Exclusion Criteria:
Women who have been diagnosed or are cervical cancer patients
Women who have been diagnosed with any cancer of the gynecological system such as cancer of the vulva, vagina, uterus, fallopian tubes and ovaries.
12. IPD Sharing Statement
Learn more about this trial
The Effect of E-health Video Towards Enhancing Cervical Cancer Screening
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