Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06788119

Analyzing the Benefits of Using SYMPTOMS-JIT for in Vivo Exposure in Anxiety Disorders: a Randomized Controlled Trial Using a Mixed Methods Approach

Led by Universitat Jaume I · Updated on 2025-05-16

158

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying anxiety disorders, including specific phobia, panic disorder, agoraphobia, and social anxiety disorder. The goal is to evaluate the effectiveness of a new smartphone-guided, sensor-based in vivo exposure therapy combined with cognitive behavioral therapy (CBT). This study compares traditional CBT with in vivo exposure to a version supported by the SYMPTOMS-JIT app, aiming to improve treatment and identify barriers to technology use in therapy. Participants will receive CBT involving psychoeducation, cognitive restructuring, emotion regulation, and coping strategies over 10 to 20 sessions. The core treatment includes repeated exposure to feared situations until distress decreases. One group receives standard in vivo exposure, while the other group uses the SYMPTOMS-JIT app to support their exposure therapy. The study includes randomized assignment to these two treatment groups. Participants will be assessed at baseline, after approximately 12 weeks of treatment, and at follow-ups after 3, 6, and 12 months. Assessments include interviews, fear and avoidance scales, and various anxiety and depression questionnaires. Researchers will monitor treatment effects, patient and therapist satisfaction, and therapy efficiency. The total participation involves initial treatment and long-term follow-up to evaluate lasting benefits and app usability.

CONDITIONS

Brief Title

Analyzing the Benefits of Using SYMPTOMS-JIT for in Vivo Exposure in Anxiety Disorders

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being at least 18 years or older.
  • Meeting DSM-5 diagnostic criteria for anxiety disorder, specifically specific phobia, agoraphobia, panic disorder, or social phobia.
  • Willingness to follow the study conditions.
  • Signing the consent form.
Not Eligible

You will not qualify if you...

  • Having another psychological problem that requires immediate attention.
  • Having current alcohol or drug dependence or abuse, psychosis, or severe organic illness.
  • Currently being treated in a similar treatment program.
  • Taking anxiolytics during the study or planning to change drug or dose during the study.

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Typically 10 to 20 sessions over up to 12 weeks

Participants receive cognitive behavioral therapy with in vivo exposure to help challenge unhelpful thoughts and behaviors, develop coping strategies, and confront feared situations repeatedly until distress decreases.

Weekly visits for up to 12 weeks

Follow-up

Duration - 12 months

Participants are monitored with assessments at 3 months, 6 months, and 12 months to evaluate the lasting effects of the treatment.

3 visits (in-person) at 3, 6, and 12 months

Trial Site Locations

Total: 1 location

1

University Jaume I

Castellon, Castellón, Spain, 12071

Actively Recruiting

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Research Team

I

Iratxe Alonso-Olea, Phd Student

J

Juana María Bretón-López, Lecturer

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Work functioning in persons with depressive and anxiety disorders: the role of specific psychopathological characteristics.

I Plaisier, A T F Beekman, R de Graaf...

https://pubmed.ncbi.nlm.nih.gov/20185180