This study will evaluate Toivoa-004 as an experimental digital therapeutic for persons with Long COVID suffering from anxiety or depression. This study will evaluate the completion rates of the Toivoa-004 program and survey the user's experience upon completion. Changes in anxiety and depression scores will be monitored during the study.
Inclusion Criteria:
Provision of signed and dated informed consent form.
Presence of clinically diagnosed Long COVID.
Stated willingness to comply with all study procedures and lifestyle considerations, and availability for the duration of the study.
Males and females; Age 22 and above.
Clinical Diagnosis of Long COVID
Willingness to adhere to the study regiment.
Access to necessary resources for participating in a technology-based intervention (i.e., Phone, internet access).
Able to read and speak English fluently.
Resident of the US and living in the US for the duration of the study.
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Exclusion Criteria:
Exploratory Study for Toivoa-001 on Human Factors
Reduction of Anxiety in People With Disabilities Through Dual Treatment: Digital CBT & NBHWC Coaching - A Randomized Clinical Trial
Reduction of Depression in People With Disabilities Through Dual Treatment: Digital CBT & NBHWC Coaching
Enhancing COVID Rehabilitation With Technology
Digital Cognitive Behavioral Therapy for Depressive Disorders
Preliminary Testing and Development of a Short Digital Intervention for Patients on Waiting Lists for Psychological Treatment
A Web-based Platform to Improve Physical Function, Nutrition, and Mindfulness in Patients With Long COVID
Cognitive Behavioral Therapy Treatment of Depression With Smartphone Support