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mHealth Behavioural Intervention to Increase Breast Cancer Screening Rates Among Members of the Public

mHealth Behavioural Intervention to Increase Breast Cancer Screening Rates Among Members of the Public

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06293508
Acronym
mBLISS-B
Enrollment
1180
Registered
2024-03-05
Start date
2024-04-30
Completion date
2024-10-04
Last updated
2024-11-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Neoplasm Female

Keywords

mHealth, breast cancer screening, behaviour, health communication, randomised controlled trial, behaviour change communication, persuasive communication, social messaging

Brief summary

Late-stage presentation of breast cancer cases are on the rise in Malaysia. Encouraging breast screening practices can assist in early breast cancer detection. Literature has proven that behavior interventions in the form of behavior change health communication using social messaging applications is a viable strategy and potentially effective at motivating breast cancer screening among the public. Such studies are scarce in the South East Asian region, particularly in Malaysia, which is the prime motivation for the current study, Based on this promising prospect, a randomized controlled trial will be designed to study the effects of applying persuasive health communication materials to initiate behavior change among a group of Malaysian women. Materials are delivered in the form of a health communication program over a social messaging application to promote breast cancer screening practices, which is either a clinical breast examination, or a mammogram. The investigators hypothesize that Malaysian women who are exposed to such materials that are designed based on behavior science and behavior change principles will be nudged and hence more likely to attend breast cancer screening compared to a control group.

Detailed description

This study involves a randomized controlled trial to asses the effectiveness of a health communication program using specifically designed materials using behavior science and behavior change principles. Materials were designed based on findings derived from a scoping review and interviewing Malaysian women through a series of qualitative interviews to determine the barriers and facilitators of attending breast cancer screening. The interview also investigated women's preferences for certain characteristics in a health message and health communication program that would motivate them to attend screening. Participants in the main experimental group will be compared with a control group, and another group which undergoes a standard health communication program.

Interventions

BEHAVIORALStandard Health Communication Intervention

Participants in this group will receive links and materials related to breast cancer screening from official sources (e.g. MOH, Non-governmental organizations (NGOs), etc.) that is already readily available and accessible by the Malaysian public. Frequency, duration, and platform of dissemination will be based on findings from Phase 1 of this study.

BEHAVIORALBehavioural Change Health Communication Intervention

Participants receive health communication materials designed using persuasive behavioural change communication principles and behavior science to promote breast cancer screening. Frequency, duration, and platform of dissemination will be based on findings from Phase 1 of this study.

Sponsors

Ministry of Health, Malaysia
CollaboratorOTHER_GOV
National University of Malaysia
CollaboratorOTHER
Institute for Health Behavioral Research, Malaysia
CollaboratorUNKNOWN
Clinical Research Centre, Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
40 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Malaysian women aged 40 years and above 2. Possess a smartphone with the predetermined social messaging application (derived from Phase 1 of study) installed. 3. Have not been diagnosed with cancer before.

Exclusion criteria

1. Underwent Clinical Breast Examination in the past 12 months. 2. Mammogram screening in the past 2 years. 3. Subjects who are deemed to have cognitive impairment and unable to provide consent to the study.

Design outcomes

Primary

MeasureTime frameDescription
Breast cancer screening attendance (either clinical breast examination (CBE) or mammogram).2 time points: 3 months after 6 month intervention period has ended, and 6 months after 6 month intervention period has ended.Self-reported attendance of breast cancer screening

Secondary

MeasureTime frameDescription
Health literacy levelAt baselineScored via a validated instrument
Perception based on domains in Health Belief Model3 time points: Baseline, 3 months after 6 month intervention period has ended, and 6 months after 6 month intervention period has ended.Scored via a validated revised Champion Health Belief Model Scale instrument
Perceived acceptance and usefulness of health communication program3 months after 6 month intervention period has ended.Scored via a validated instrument
Reasons behind participants not participating in breast cancer screening.2 time points: Baseline, and 3 months after 6 month intervention period has ended.Determined via a multiple choice question

Countries

Malaysia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026