The Research
Aakhyān is being evaluated through a pilot randomized controlled trial at Silchar Cancer Centre, Assam.
Study Progress
Protocol
Study protocol finalised. Prospective, assessor-blinded, parallel-group pilot RCT with stratified block randomisation.
Protocol Preprint
Protocol paper published on medRxiv (April 2026). doi:10.64898/2026.04.15.26350965
Ethics (IEC)
Institutional Ethics Committee approval — application submitted.
CTRI Registration
Clinical Trials Registry of India — follows IEC approval.
Enrolment
100 patients (50 intervention, 50 control). Estimated 10–14 week enrolment period.
Results
30-day follow-up per patient. Preprints will be published on this page.
Publications
Preprint
Aakhyan: An AI-Powered Vernacular Patient Communication Platform for Oncology in Resource-Limited Settings — System Architecture and Pilot Randomised Trial Protocol
Purkayastha, D. S. (2026). medRxiv. doi:10.64898/2026.04.15.26350965
Study Design
Prospective, randomised, controlled, single-centre, open-label preliminary efficacy and feasibility study with stratified block randomisation by discharging consultant. 100 oncology patients (50 intervention, 50 standard care) at Silchar Cancer Centre, Assam. Reported per CONSORT extension for pilot and feasibility trials and WHO mERA checklist.
Intervention Group
Standard discharge + Aakhyān WhatsApp voice messages (6-message discharge sequence, medication nudges, follow-up reminders). Structured teach-back at 48–72 hours.
Control Group
Standard discharge only (printed summary + verbal explanation). Same teach-back assessment at 48–72 hours for comparison.
Primary Outcome
Discharge instruction comprehension at 48–72 hours post-discharge, measured by structured teach-back assessment.
Five domains, each scored 0–2 (total 0–10):
- Medications — can the patient name their medications and what each one is for?
- Frequency/Timing — does the patient know how many times a day and when to take each medicine?
- Food relation — does the patient know which medicines to take before or after food?
- Red flags — can the patient name warning signs that should bring them back to hospital?
- Follow-up — does the patient know when their next appointment is and what to bring?
Adequate comprehension: score of 7 or higher, with a safety-floor rule — a score of 0 on dosing schedule or warning signs domains counts as inadequate regardless of total.
Secondary Outcomes
System Feasibility
- Pipeline completion rate (target: ≥90%)
- Median approval time (target: ≤30 minutes)
- Message delivery rate (target: ≥95%)
- Patient engagement (target: ≥40%)
- Patient opt-out rate (target: ≤10%)
Clinical (Exploratory)
- Follow-up attendance and timeliness
- Pre-investigation completion
- 30-day emergency department visits
- Self-reported medication adherence
- Patient and caregiver satisfaction
Protocol Details
- Study Title
- Aakhyan: Preliminary Clinical Efficacy and Feasibility of an AI-Powered Vernacular Patient Communication System for Oncology Patients
- Reporting Standards
- CONSORT extension for pilot and feasibility trials · WHO mERA checklist · DPDPA 2023 compliance documentation
- Follow-up
- 30 days per patient
- Status
- Protocol finalised. IEC application submitted. Enrolment commencing 2026.
This is a pilot trial — preliminary evidence from 100 patients at a single centre, designed to inform a future multi-centre study. Results will be published on this page as the pilot progresses.
For the post-discharge communication architecture being evaluated in this pilot, see The Platform. For the clinician workflow, see For Clinicians. For regulatory alignment, see NABH Standards.