Clinical trial Recruiting at 1 site Observational Ages 5 and up

Home-based mobile neurological check for people with brain tumors

Official title: Self-administered Remote Neurological Examination Using Mobile Application in Patients With Brain Tumors

Run by Tata Memorial Centre · NCT07236840 · Data updated 2026-11-12

This project will test whether people with brain tumors older than 5 can use the Iskhaa Android app to do guided self-neurological exams, upload short videos, and have an AI model detect changes that might predict neurological worsening.

Quick facts

Study typeObservational
Ages5 Years and up
SexAll
Enrollment600 (estimated)
SponsorTata Memorial Centre
Academic / other
Locations1 site (Mumbai, Maharashtra)
StatusRecruiting
StartedFebruary 20, 2026
Main results expectedNovember 1, 2027
Study endsNovember 5, 2027
Registry record updatedFebruary 24, 2026
Trial IDNCT07236840 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are people aged over 5 with a radiologic or histologic diagnosis of a brain tumor, an expected survival over six months, able to follow app instructions, and who or whose caregiver can install and use an Android smartphone app.

Probably not a fit

Patients with severe cognitive or psychiatric impairment, KPS/LPS below 50, expected survival under six months, unreliable caregivers, or no access to a compatible Android smartphone are unlikely to benefit from this approach.

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

What this trial studies

This observational study develops and deploys the Iskhaa mobile application to guide patients through self-administered neurological tasks (speech, gait, limb movements) with pre-recorded video instructions and video recording. Data and videos will be stored on a secure hospital server and reviewed by investigators via mobile or desktop interfaces, while participants also complete EORTC QLQ-C30 and BN20 quality-of-life questionnaires. An AI model will be trained and validated on the recorded features to detect functional changes and predict subsequent neurological deterioration. The initial phase includes supervised onsite use (about 100 participants) at Tata Memorial Centre with subsequent remote use for eligible participants.

Why it matters

Potential benefit: If successful, the app plus AI could enable earlier detection of neurological decline and more convenient remote monitoring for people with brain tumors.

How similar studies have gone: Smartphone and video-based neurological assessments have shown promise in other neurological conditions, but using recorded videos plus AI to predict deterioration specifically in brain tumor patients remains largely exploratory.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Diagnosis of brain tumors (histopathology/ radiology).
2. Age \> 5 years
3. Patient or caregiver have access to an android smart phone and is able to install the mobile application.
4. Expected survival more than 6 months during study accrual.
5. Signing patient consent or parent consent/ child assent form (as appropriate).

Exclusion Criteria:

1. Patient or caregiver is not reliable to follow instructions or use the mobile application.
2. Patient with severe cognitive or psychiatric issues causing difficulty in using the app or follow instructions.
3. Karnofsky Performance Status (KPS) or Lansky Performance Status LPS) \<50.
4. Terminal illness with expected life expectancy (\<6 months).

Where it's running

  • Tata Memorial Centre
    Mumbai, Maharashtra, India
    Recruiting

Study contacts

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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.
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.