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Clinical Trial Summary

This study is a 6-month follow-up study to WB001-001 conducted to assess and evaluate the durability of the effect of {WB001+TAU} beyond the 8-week treatment period.

Clinical Trial Description

This study is a 6-month prospective, observational follow-up study to the WB001-001 trial. Participants will be a convenience sample of those enrolled in the WB001-001 parent trial who consent to participate in a follow-up study at baseline for WB001-001. After completion of WB001-001's EOT assessment, those consenting to participate in the current study will be screened to confirm eligibility. Eligible participants will complete six assessment batteries (patient-reported outcomes [PROs]) on a monthly basis for a 6-month observation period. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05693792
Study type Observational
Source Woebot Health
Contact Athena Robinson, PhD
Phone (415) 209-5642
Status Not yet recruiting
Start date February 1, 2023
Completion date June 8, 2024

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