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NCT06729164

Strategic and Interactive Signing Instruction Experiment

Active, enrolled NA Last updated 24 November 2025
What this trial tests

NA trial testing Strategic and Interactive Signing Instruction in Sign Language Skills in 150 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
1 April 2025
Primary endpoint
30 July 2026
30 July 2026

Quick facts

Lead sponsorThe University of Tennessee, Knoxville
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment150
Start date1 April 2025
Primary completion30 July 2026
Estimated completion30 July 2026
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The University of Tennessee, Knoxville

Who can join

Adults 4 to 12, any sex, with Sign Language Skills or Teacher Practice. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This RCT study involves teachers divided into an experimental group and a control group. Teachers in the experimental group will receive SISI training to support the sign language development of deaf children, while those in the control group will continue with "business-as-usual" teaching methods. Pre- and post-assessments will be conducted for all deaf children at the beginning and end of the school year.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Strategic and Interactive Signing Instruction

Trials testing the same drug.

Other recruiting trials for Sign Language Skills

Currently open trials in the same condition.

Other The University of Tennessee, Knoxville trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT06729164.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing