Cervical Cancer ScreeningNCT05426642
The Effect of E-health Video Towards Enhancing Cervical Cancer Screening
A study testing E-health Video KaSEH and Brochure in people with Cervical Cancer Screening, run by Universiti Kebangsaan Malaysia Medical Centre.
Trial 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. Read more about this study
- Who is it for?
- Ages 21 to 65 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Cervical Cancer Screening
- What is being tested?
- E-health Video KaSEH and Brochure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- No sites listed yet
- Study dates
- Mar 2023to Oct 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 to 65 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Women who have never undergone cervical cancer screening.
Who cannot join
- 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.
About this study
Official title: Development and Evaluation of KaSEH Video to Increase Women's Knowledge and Motivation Regarding Cervical Cancer and Its Screening.
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.
- Conditions
- Cervical Cancer Screening
- Being tested
- E-health Video KaSEH, Brochure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
E-health Video KaSEHOther
The e-health video KaSEH is produce based on Protection Motivation Theory to enhance women's motivation towards cervical cancer screening.
BrochureOther
The brochure contain the information regarding cervical cancer and its screening
| Study group | Role | What they receive |
|---|---|---|
| Intervention group | Experimental | Receive the e-health video and brochure as the intervention Receives: Other: E-health Video KaSEH; Other: Brochure |
| Control group | Other | Receive brochure as the intervention Receives: Other: Brochure |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: 3 month
Practice
Measured by yes (uptake of cervical cancer screening) and no (did not perform screening).
Measured: 3 month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2022
- Study startMar 2023 (estimated)
- Primary completionSep 2023 (estimated)
- Study completionOct 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cervical Cancer ScreeningStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universiti Kebangsaan Malaysia Medical Centre
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05426642
- Sponsor's protocol ID
- FF-2021-499
- Status last verified
- Jun 2022
- First submitted
- 15 Jun 2022
- Last updated
- 22 Jun 2022
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Romli R, Mohammed Nawi A, Abd Rahman R, Mohamad EMW, Chew KT, Mohd Hashim S. Digital motivation for cervical cancer screening: A quasi-experimental trial of the SeDAR Video among middle adulthood Malaysian women. PLoS One. 2026 May 20;21(5):e0347489. doi: 10.1371/journal.pone.0347489. eCollection 2026.
PubMed 42160295
Study at a glance
From the registry record, last updated by the sponsor on 22 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Development and Evaluation of KaSEH Video to Increase Women's Knowledge and Motivation Regarding Cervical Cancer and Its Screening.
- ClinicalTrials.gov ID
- NCT05426642
- Acronym / sponsor ID
- FF-2021-499
- Conditions
- Cervical Cancer Screening
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Universiti Kebangsaan Malaysia Medical CentreUniversity, hospital or other
- Study start
- Mar 2023 (estimated)
- Primary completion
- Sep 2023 (estimated)
- Study completion
- Oct 2023 (estimated)
- First posted
- 22 Jun 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention group | Experimental | Other: E-health Video KaSEH, Other: BrochureReceive the e-health video and brochure as the intervention |
| Control group | Other | Other: BrochureReceive brochure as the intervention |
Who may qualify
- Ages
- 21 to 65 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Women who have never undergone cervical cancer screening.
Key exclusion criteria (2 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| E-health Video KaSEHThe e-health video KaSEH is produce based on Protection Motivation Theory to enhance women's motivation towards cervical cancer screening. | Other | Intervention group |
| BrochureThe brochure contain the information regarding cervical cancer and its screening | Other | Control group, Intervention group |
Primary outcome
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).
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Jun 2022.
- Derived from this study: PubMed 42160295Romli R, Mohammed Nawi A, Abd Rahman R, Mohamad EMW, Chew KT, Mohd Hashim S. Digital motivation for cervical cancer screening: A quasi-experimental trial of the SeDAR Video among middle adulthood Malaysian women. PLoS One. 2026 May 20;21(5):e0347489. doi: 10.1371/journal.pone.0347489. eCollection 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A study testing E-health Video KaSEH and Brochure in people with Cervical Cancer Screening, run by Universiti Kebangsaan Malaysia Medical Centre.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 22 Jun 2022. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Motivation level (time frame: 3 month). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05426642, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jun 2022.