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mSaada: A Mobile Health Tool

mSaada: A Mobile Health Tool

Recruiting
18 years and older
All
Phase N/A

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Overview

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.

Eligibility

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

Exclusion Criteria:

  • Does not understand the study purpose and details
  • Is not willing to provide informed consent

Aim 2 Community health volunteers (CHVs)

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
  • intact cervix and uterus
  • able to provide informed consent.

Exclusion Criteria:

  • Does not understand the study purpose and details
  • Is not willing to provide informed consent

R33

Eligibility criteria for women participants include:

  1. reside within Kisumu County,
  2. have access to government health facilities with capacity to provide HPV testing,
  3. are eligible for cervical cancer screening per the Kenya Ministry of Health guidelines (women who are between ages 30-65 and have an intact uterus and cervix) and
  4. ability to provide informed consent.

Eligibility criteria for CHV participants include:

  1. reside within Kisumu County,
  2. work in government health facilities that deliver cervical cancer screening and treatment to women, and 3) ability to provide informed consent.

Study details
    Cervical Cancer
    HPV
    mHealth

NCT05848557

Duke University

15 October 2025

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