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The Effect of E-health Video Towards Enhancing Cervical Cancer Screening

Sponsor
Universiti Kebangsaan Malaysia Medical Centre (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05426642
Collaborator
(none)
60
Enrollment
2
Arms
7
Anticipated Duration (Months)

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: E-health Video KaSEH
  • Other: Brochure
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Screening
Official Title:
Development and Evaluation of KaSEH Video to Increase Women's Knowledge and Motivation Regarding Cervical Cancer and Its Screening.
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Receive the e-health video and brochure as the intervention

Other: E-health Video KaSEH
The e-health video KaSEH is produce based on Protection Motivation Theory to enhance women's motivation towards cervical cancer screening.

Other: Brochure
The brochure contain the information regarding cervical cancer and its screening
Other: Control group

Receive brochure as the intervention

Other: Brochure
The brochure contain the information regarding cervical cancer and its screening

Outcome Measures

Primary Outcome Measures

  1. Motivation level [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.

  2. Practice [3 month]

    Measured by yes (uptake of cervical cancer screening) and no (did not perform screening).

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 65 Years
Sexes Eligible for Study:
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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Universiti Kebangsaan Malaysia Medical Centre

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Universiti Kebangsaan Malaysia Medical Centre
ClinicalTrials.gov Identifier:
NCT05426642
Other Study ID Numbers:
  • FF-2021-499
First Posted:
Jun 22, 2022
Last Update Posted:
Jun 22, 2022
Last Verified:
Jun 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Uterine Cervical Neoplasms

Study Results

No Results Posted as of Jun 22, 2022