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Determining the most effective combination of patient navigation strategies to reduce loss-to-follow-up in the cervical cancer screening pathway in Tanzania

Evaluating the most effective ‘package’ of mHealth supported patient navigation strategies to encourage cervical cancer screening among HPV+ women and reduce the number of women lost-to-follow-up in Kilimanjaro, Tanzania

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202307605212308
Enrollment
2000
Registered
2023-07-31
Start date
2023-09-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Cancer

Interventions

Enhanced usual care
Nurse navigation plus enhanced usual care
App navigation plus enhanced usual care
Nurse navigation plus app navigation plus enhanced usual care

Sponsors

Queens University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: The inclusion criteria for participants is the following: - Gender: person with an intact cervix - Age: 25 (if HIV positive) and/or age 30 to 49 years old at the time of enrollment as reported verbally - Residence in the study-defined catchment area - Language: able to speak/understand English (preferred) or Kiswahili (if the participant cannot read the consent will be read to her and a thumbprint will suffice for consent) The inclusion criteria for the CHWs is the following: - Women - Physically fit/ambulatory - Secondary school completion (preferred) - Can read and write in Kiswahili and ‘basic’ English - Experience using Android smartphone/tablets (preferred) - Can be trained to perform informed consent process The inclusion criteria for the providers is the following: - CECAP provider of a CECAP site in the Kilimanjaro region - Participated in previous SEVIA training (familiar with cervical images and review process) - Can read and write in Kiswahili and English - Experience using technology/tablets (preferred)

Exclusion criteria

Exclusion criteria: The exclusion criteria for the women is the following: - Current pregnancy (if verbally reported as currently pregnant or possibly pregnant) - History of cervical cancer - History of hysterectomy - Unwilling to collect vaginal specimen for any reason (note that menstrual bleeding is not a contraindication if women are willing to collect the specimen while bleeding) - Apparent inability to give informed consent - Unwillingness to participate

Design outcomes

Primary

MeasureTime frame
The primary outcome is women attending VIA within 6 weeks of receiving a positive HPV result. Women will be randomized at the time they receive a phone call to tell them that their result has been processed.

Secondary

MeasureTime frame
The proportion of navigation checkpoints that each woman completes in their unique care/treatment pathway (e.g., completion of thermal ablation), 6 months after attending VIA.

Countries

Tanzania

Contacts

Public ContactGaudensia Olomi

Regional Nursing Officer and Local Program Manager

g.olomi@kcri.ac.tz+255756831210

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026