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NCT05822999

Study of Efficacy of WELT-IP in Insomnia (WCTP-I-B-01)

Completed NA Last updated 21 April 2023
What this trial tests

NA trial testing WELT-IP in Insomnia in 52 participants. Completed in 8 June 2022.

Timeline
15 December 2021
Primary endpoint
26 April 2022
8 June 2022

Quick facts

Lead sponsorWELT corp
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment52
Start date15 December 2021
Primary completion26 April 2022
Estimated completion8 June 2022
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

WELT corp

Who can join

Adults 19 to 65, any sex, with Insomnia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study was to determine safety and efficacy of WELT-IP in adult insomnia patients. WELT-IP is a cognitive behavioral therapy for insomnia (CBT-I) based digital therapeutics.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Impact of Adherence to Digital Cognitive Behavioral Therapy for Insomnia Effectiveness.
    Lee S, Park KM, Lee DH, Choi EC, et al · · 2025 · cited 1× · PMID 40992766 · DOI 10.3349/ymj.2024.0398
  2. Culturally adapted digital cognitive behavioral therapy for insomnia in South Korea - a double-blind randomized controlled trial.
    Kabbani A, Passler M, Park K, Lee E, et al · · 2026 · PMID 41883996 · DOI 10.1016/j.invent.2026.100933

Verify or expand the search:

Other trials of WELT-IP

Trials testing the same drug.

Other recruiting trials for Insomnia

Currently open trials in the same condition.

Other WELT corp 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/NCT05822999.

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