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Evaluation of mobile phone application for primary screening of women for cervical Pre-cancer / cancer in limited resource areas

Evaluation of ColpPhonTM application for outreach screening environment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/09/005003
Enrollment
230
Registered
2014-09-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Women who are aged between 30-65 years with completely visible cervix and also have sexual history more than 1 year

Interventions

Intervention1: ColpPhoneTM: Mobile Phone app for cervical cancer screening Control Intervention1: Colposcopy: A procedure to closely examine your cervix, vagina and vulva for signs of disease.

Sponsors

Philips India Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Intact cervix • Female subjects who are married for at least 1 year

Exclusion criteria

Exclusion criteria: • Female subjects with age 30 years or 65 years( as per Asha Jyoti inclusion criteria) • No cervix/ cervix not visible e.g. post hysterectomy cases • Pregnant women • Iodine allergy

Design outcomes

Primary

MeasureTime frame
To evaluate the image quality on clinical cases examined by ColpPhonTM compared to Colposcopy for identifying women with potential cervical pre-cancer in a mobile healthcare outreach scenario.Timepoint: 3 Months—

Secondary

MeasureTime frame
To obtain feedback from healthcare worker and Gynecologist on the usability aspects of the ColpPhonTM application along with the mobile setup including its technical and clinical feasibilityTimepoint: 3 Months—

Countries

India

Contacts

Public ContactDr Payal K

Study Manager

Keswarpu.payal@philips.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026