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mSaada: A Mobile Health Tool

mSaada: A Mobile Health Tool to Improve Cervical Cancer Screening in Western Kenya

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05848557
Enrollment
6000
Registered
2023-05-08
Start date
2024-02-19
Completion date
2027-06-30
Last updated
2026-08-13

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

Conditions

Cervical Cancer, HPV, mHealth

Brief summary

In the R21 phase of this project, investigators will: (1) work with key stakeholders and local and international developers to finalize the mSaada platform, building on the existing prototype to add patient and specimen tracking functionality; and (2) carry out a pilot to identify the patient, provider and health system factors necessary to design a trial to evaluate mSaada effectiveness in assisting community health volunteer-led home-based HPV screening, and implementation factors. Investigators will carry out a six-month pilot of mSaada with community units in two health facilities providing HPV-based screening, and use performance metrics including system usage rates, workflow observations and qualitative data to guide the planning of a to determine effectiveness. In the R33 phase of the project, investigators plan to: (1) conduct an 18-month c-RCT across 12 health facilities to determine the impact of mSaada on cervical cancer screening uptake, treatment acquisition and cervical cancer knowledge levels among women in the community; and (2) measure the requisite implementation factors for mSaada effectiveness, sustainability, and scale-up. The rigorous study design will allow us to determine the clinical impact of mSaada, ensure the local and regional infrastructure has the capacity necessary for sustainability and develop strategies for widespread implementation and scale-up. Collaboration with key stakeholders from the Kenya Ministry of Health will facilitate the development of a long-term sustainability plan as the country moves toward HPV-based cervical cancer screening. Investigators anticipate the mSaada platform will play a pivotal role in facilitating the introduction of HPV-based screening programs that can reach women in settings with limited health care infrastructure.

Interventions

BEHAVIORALmSaada

mSaada is an integrated digital platform to support patients, community health volunteers (CHVs), providers and health systems in an HPV-based cervical cancer screening strategy. mSaada is hosted on an open-source platform (Dimagi, CommCare) as a mobile health application to support patient data collection, protocol support and counseling aids. mSaada will include an education module, patient and specimen tracking, screening reminders, and messaging functionality.

Sponsors

Duke University
Lead SponsorOTHER
National Cancer Institute (NCI)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

R21 Aim 1 Community health volunteers (CHVs), facility providers and supervisors, Ministry of Health officials Inclusion Criteria: * 18 years or older * be employed by a government clinic * be working in cervical cancer screening

Exclusion criteria

* Does not understand the study purpose and details * Is not willing to provide informed consent Women Inclusion Criteria: \- between 30 and 65 years old

Design outcomes

Primary

MeasureTime frameDescription
Number of Community Health Volunteers (CHVs) reporting a usability score greater than 601-daymSaada Usability Survey with a range of 20-100, where a higher score indicates a higher level of acceptability (mean scores \>60 is considered acceptable).
Proportion of women in each arm who complete cervical cancer screening1-dayCalculated by dividing the number of women screened by the number of eligible women attending health facilities
Proportion of women in each arm who test HPV-positive and access treatment within 3 months of receiving their results1-dayCalculated the number of women treated within 3 months of receiving their results by dividing the number of women who test HPV positive
Difference in women's knowledge level of cervical cancer as measured by a knowledge scale between the arms1-dayThe knowledge scale has a score range of 0 to 5, where a higher score indicates a higher level of knowledge.
Difference in women risk perception of cervical cancer as measured by a risk perception scale between the arms1-dayThe Risk Perception Scale has 3 Likert scale questions regarding risk perception.
Difference in Community Health Promoter (CHP) screening self-efficacy, knowledge, usability between the arms1-dayQuantitative self-efficacy, knowledge and usability survey with CHPs after participating in the study..

Countries

Kenya

Contacts

CONTACTMegan Huchko, MD, MPH
megan.huchko@duke.edu919 613 5062

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026