NCT05426642

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 15, 2022

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 22, 2022

Completed
8 months until next milestone

Study Start

First participant enrolled

March 1, 2023

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2023

Completed
Last Updated

June 22, 2022

Status Verified

June 1, 2022

Enrollment Period

6 months

First QC Date

June 15, 2022

Last Update Submit

June 20, 2022

Conditions

Cervical Cancer Screening

Outcome Measures

Primary Outcomes (2)

  • 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.

    3 month

  • Practice

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

    3 month

Study Arms (2)

Intervention group

EXPERIMENTAL

Receive the e-health video and brochure as the intervention

Other: E-health Video KaSEHOther: Brochure

Control group

OTHER

Receive brochure as the intervention

Other: Brochure

Interventions

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.

Intervention group
BrochureOTHER

The brochure contain the information regarding cervical cancer and its screening

Control groupIntervention group

Eligibility Criteria

Age21 Years - 65 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Women who have never undergone cervical cancer screening.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SCREENING
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 15, 2022

First Posted

June 22, 2022

Study Start

March 1, 2023

Primary Completion

September 1, 2023

Study Completion

October 1, 2023

Last Updated

June 22, 2022

Record last verified: 2022-06