Clinical trial Recruiting at 1 site Observational Ages 18 and up

From exclusion to inclusion: understanding and reconnecting breast cancer patients who stopped follow-up

Official title: A Comprehensive Analysis of Follow-up Outcomes, Continuity and Updated Survivorship in Breast Cancer

Run by Basavatarakam Indo American Cancer Hospital & Research Institute · NCT06927102 · Data updated 2026-11-12

This project will try outreach by phone, message, or email to see if women treated for non-metastatic breast cancer at a Hyderabad tertiary centre who stopped follow-up can be re-engaged.

More Breast Carcinoma trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1500 (estimated)
SponsorBasavatarakam Indo American Cancer Hospital & Research Institute
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Hyderabad, Telangana)
StatusRecruiting
StartedMay 1, 2025
Main results expectedSeptember 2025
Study endsOctober 2025
Registry record updatedSeptember 19, 2025
Trial IDNCT06927102 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women diagnosed with non-metastatic breast cancer between 2017 and 2018 who were treated at Basavatarakam Indo American Cancer Hospital and are currently classified as lost-to-follow-up and willing to re-engage.

Probably not a fit

Patients who have permanently relocated outside the study region, received ongoing care at another centre, have incomplete records, or cannot be contacted are unlikely to benefit from the outreach approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a prospective cohort analysis of women diagnosed with non-metastatic breast cancer in 2017–2018 who received treatment at a single tertiary cancer centre. Baseline demographic, tumor, stage, subtype, and treatment data will be collected from medical records. Phase I will document annual follow-up visits through December 2024 using hospital records and EMR to determine five-year loss-to-follow-up rates and associated factors. Phase II will identify patients categorized as lost-to-follow-up, extract additional socioeconomic and geographic variables, and undertake proactive outreach to obtain consent, current health status, and patient-reported barriers to follow-up.

Why it matters

Potential benefit: If successful, proactive outreach could bring more patients back into follow-up care, enabling earlier detection of recurrence and improved long-term management.

How similar studies have gone: Similar proactive outreach programs have reduced loss-to-follow-up in other cancer and chronic disease settings, though robust local evidence from Indian tertiary centres is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients newly diagnosed with non-metastatic breast cancer between 2017-2018
2. Patients categorized as "lost-to-follow-up", as defined above
3. Patients willing to participate upon re-engagement

Exclusion Criteria:

1. Patients with incomplete medical records
2. Patients who have taken part of the treatment at another hospital/centre
3. Patients who have relocated permanently out of the study region

Withdrawal Criteria:

1\. Patient withdraws consent

Where it's running

  • Basavatarakam Indo American Cancer Hospital & Research Institute
    Hyderabad, Telangana, India
    Recruiting

Study contacts

  • Principal investigator: Nisha Hariharan, MS,HBNI Fellow Breast Oncology — Basavatarakam Indo American Cancer Hospital & Research Institute
  • Study coordinator: Clinical Trial Co-ordinator, Pharm D
  • Email: research.oncology@basavatarakam.org
  • Phone: 040-23551235

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Browse more
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.