18 and older, any sex, with Feasibility or Acceptability. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Feasibility of the InterventionPrimary· Post-intervention at 5 month endline survey
Proportion of participants who complete 50% of the intervention sessions
Group
Value
95% CI
TARANG Arm
28
AcceptabilityPrimary· Post-intervention at 5 month endline survey
Proportion of participants who were completely or somewhat satisfied with the intervention
Group
Value
95% CI
TARANG Arm
34
UsefulnessPrimary· Post-intervention at 5 month endline survey
Proportion of participants who found the TARANG intervention sessions very useful or somewhat useful
Group
Value
95% CI
TARANG Arm
35
Sponsor's own description
The mixed methods pilot study aims to evaluate the acceptability, feasibility, and implementation challenges of the TARANG intervention in villages in rural/tribal Rajasthan to inform the study design and operational details for a larger cluster-randomized controlled trial.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of California, San Francisco
Last refreshed: 6 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06320964.