Development and Evaluation of KaSEH Video to Increase Women's Knowledge and Motivation Regarding Cervical Cancer and Its Screening.
Trial Snapshot
- Phase
- Not Applicable
- Sponsor
- Enrollment
- 60
- Primary Endpoint
- Motivation level
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Screening
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 21 Years to 65 Years (Adult, Older Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
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.
Arms & Interventions
Intervention group
Receive the e-health video and brochure as the intervention
Intervention: E-health Video KaSEH (Other)
Intervention group
Receive the e-health video and brochure as the intervention
Intervention: Brochure (Other)
Control group
Receive brochure as the intervention
Intervention: Brochure (Other)
Outcomes
Primary Outcomes
Motivation level
Time Frame: 3 month
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
Time Frame: 3 month
Measured by yes (uptake of cervical cancer screening) and no (did not perform screening).
Secondary Outcomes
No secondary outcomes reported