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Clinical Trials in Spain / NCT06788119
Recruiting Not applicable

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

NCT06788119 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2025-04-30
Last updated
2025-05-16

Condition(s) studied

Anxiety DisordersSpecific PhobiaPanic DisorderAgoraphobiaSocial Anxiety Disorder

Investigational drug(s) / intervention(s)

Cognitive behavioral therapy with in vivo exposureCognitive behavorial therapy with in vivo exposure plus SYMPTOMS-JIT

Cognitive behavioral therapy with in vivo exposure: CBT will be used as the chosen approach for ADs. The main components will be psychoeducation and to help patients to challenge and change unhelpful cognitive distortions (e.g., thoughts, beliefs, and attitudes) and behaviors (e.g., avoidance), develop emotion regulation strategies (e.g., cognitive reappraisal), and learn coping strategies that target problem-solving. The practice is developed in several sessions that usually last between 10 and 20 sessions. Specifically, the exposure component will be considered as the first-line treatment. During the exposure component, patients will confront themselves over a long period of time, repetitively, with a feared stimulus until distress has decreased significantly by the exposure.In this condition participants will receive CBT treatment and be exposed to in vivo situations.

Cognitive behavorial therapy with in vivo exposure plus SYMPTOMS-JIT: CBT will be used as the chosen approach for ADs. The main components will be psychoeducation and to help patients to challenge and change unhelpful cognitive distortions (e.g., thoughts, beliefs, and attitudes) and behaviors (e.g., avoidance), develop emotion regulation strategies (e.g., cognitive reappraisal), and learn coping strategies that target problem-solving. The practice is developed in several sessions that usually last between 10 and 20 sessions. Specifically, the exposure component will be considered as the first-line treatment. During the exposure component, patients will confront themselves over a long period of time, repetitively, with a feared stimulus until distress has decreased significantly by the exposure. In this condition participants will receive CBT treatment and be exposed to in vivo situations with the support of SYMPTOMS-JIT.

Study summary

The aim of this study is to develop and test the efficacy of first-of-its-kind, fully instrumented sensor-based smartphone-guided in-vivo exposure therapy using a just-in-time intervention for anxiety disorder. The main hypotheses are:

1. Both treatment conditions (CBT treatment with IVE and CBT treatment with IVE+SYMPTOMS-JIT) will show efficacy and no statistically significant differences will be found between them. The efficacy will be determined for the differences in pre-post treatment in the used outcome measures.
2. The therapeutic gains obtained in both treatment conditions (IVE and (IVE+SYMPTOMS-JIT) will be maintained at 1-, 6-, and 12-month follow-up periods.
3. Both treatment conditions will be efficient, that is, they will be well-valued by patients and therapists. However, IVE+SYMPTOMS-JIT will be preferred and perceived as less aversive than IVE.
4. The main barriers for the use of this technology are not technological, but rather attitudinal and they can be identified through qualitative studies.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Being at least 18 years or older. * Meeting DSM-5 diagnostic criteria (APA, 2013) for anxiety disorder, specifically specific phobia, agoraphobia, panic disorder and social phobia. * Being willing to follow the study conditions. * Sign the consent form. Exclusion Criteria: * 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 in the case of taking them, changing drug or dose during the study).

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University Jaume I Castellon Castellón Recruiting

More Universitat Jaume I trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06788119 on ClinicalTrials.gov ↗ ← All trials in Spain