Dass-167 -

A Phase 2 clinical trial is currently underway to evaluate the efficacy and safety of DASS-167 in patients with mild to moderate COVID-19. The study aims to enroll patients from various sites worldwide and will assess the clinical outcomes, viral load, and safety of DASS-167 compared to standard of care.

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The code refers to a specific informative session and task within a larger neurocognitive research study. This session serves as the entry point for participants, designed to ensure they understand the project's rationale, objectives, and procedures before moving on to treatment and assessment. The Role of DASS-167 in Research DASS-167

: Ensure your journal page or canvas is completely dry. If you used watercolors or heavy ink, allow them to set so no moisture is trapped under the non-porous PET layer.

The DASS-167 was developed in the late 1990s by a team of researchers led by Dr. Syd Lovibond and Dr. Peter Lovibond. The original version of the DASS, known as the DASS-21, was a 21-item questionnaire designed to assess the severity of depression, anxiety, and stress in adults. However, in 2003, the DASS-167 was developed as a longer and more comprehensive version of the DASS-21. The DASS-167 consists of 167 items, making it one of the most comprehensive psychological assessment tools available. A Phase 2 clinical trial is currently underway

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The DASS-167 has demonstrated excellent psychometric properties, including: The Role of DASS-167 in Research : Ensure

The DASS-167 has a wide range of applications in both clinical and research settings:

Each item is rated on a 4-point Likert scale, ranging from 0 (did not apply to me at all) to 3 (applied to me very much, or most of the time). The subscales can be scored separately, providing a profile of an individual's mental health symptoms.

Toxicity studies were conducted in rodents and non-human primates to assess the safety of DASS-167. The compound was generally well-tolerated, with no evidence of significant toxicity or adverse effects.