Examining the Effectiveness of Wysa for Worry Program

Wysa

Status

Not yet enrolling

Conditions

Anxiety

Treatments

Behavioral: Wysa for Worry

Behavioral: App-based Psychoeducation

Study type

Interventional

Funder types

Industry

Identifiers

NCT05943418

Wysa_RCT_01

Details and patient eligibility

About

The goal of this randomized controlled trial is to test for the effectiveness of Wysa's Worry computerized cognitive behaviour therapy (cCBT) program (a digital mental health intervention) in comparison to a digital app that offers psychoeducation to patients who have mild to moderate symptoms of anxiety.

Full description

People dealing with worry can receive augmented support from digital mental health interventions. The intervention being tested in this study is Wysa's Worry cCBT program. Its outcomes will be compared to a randomized, controlled arm that offers psychoeducation.

For the purpose of this study participants will be recruited through different online channels and will be randomly assigned to either the intervention or control group. Regardless of their assignment they will be completing weekly standardized assessments examining their symptoms of anxiety and depression, and examining any improvement.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

The inclusion criteria for the study is as follows:
- Patients who are at least 18 years of age.
- Patients who have mild to moderate symptoms of anxiety (scores: 5-15, according to GAD-7).
- Patients who are not already engaged in psychological therapy and not intending to start psychological therapy in the next eight weeks.
- Patients who haven't used any DMHI (Digital Mental Health Interventions) in the last 6 months.
- Patients without risk of suicidal ideation and behaviour.
- Patients who are capable of reading and understanding English and have provided written or verbal informed consent to participate.
- Patients who own and use a smartphone with functional audio.

Exclusion criteria

Patients who are at an increased risk of suicide.
Patients with diagnosis of or receiving treatment for alcohol/substance use disorder.
Patients who've had their psychiatric medication or dose changed in the last 1 month.
Patients who suffer from severe anxiety
Patients with diagnosis of or receiving treatment for an active state of psychosis.