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Not yet recruiting NCT06767878

Internet Delivered Therapy for Social Anxiety in Adults

No phase Interventional Control Group Intervention

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: PORTiSOFIE.
Who it may be relevant to
Registry conditions: Control Group, Intervention. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Portugal
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Internet Delivered Therapy for Social Anxiety in Adults (PORTiSOFIE): Study Protocol for a Randomized Controlled Trial

Overview

The goal of this clinical trial is to learn if an internet-delivered CBT protocol for social anxiety in adults (PORTiSOFIE) is effective in Portugal. It will also learn about the impact that PORTiSOFIE may have on relationship dimensions of these individuals. The main questions it aims to answer are: Does PORTiSOFIE is effective? What impact PORTiSOFIE has in relationship dimensions? Participants will: Be assigned to experimental group and receive intervention briefly after screening is complete; Or control group and only receive intervention after the experimental group finishes.

Detailed description

Social Anxiety Disorder (SAD) is a common condition that affects intrapersonal (e.g., distress and impairment) and interpersonal functioning (e.g., difficulties in amorous relationships). People with SAD tend to have difficulties in communicating feelings with partners and report lower levels of relationship and sexual satisfaction. Cognitive behavioral therapy (CBT) for SAD has been found to redcuce symptoms of social anxiety, but less is known about its impact on relationship functioning. Internet-based CBT (iCBT) has gained attention for its primary advantage bridging distances and saving time for the patient. In the planned study the investigators aim to translate and culturally adapt an iCBT program for social anxiety for use in Portugal (PORTiSOFIE) and measure the effects of the program on social anxiety symptoms. The project will also study the impact on relationship satisfaction and other relevant outcomes. The investigators will conduct a randomized controlled trial and divide participants in a two-arm study with parallel groups (i.e., intervention group and wait-list group). Participants will answer questionnaires to assess social anxiety symptoms and relationship outcomes at pre-treatment, posttreatment and 6-month follow up. Participants partner's will also be asked to complete questionnaires on the same periods of time, but only regarding relationship outcomes. iCBT for SAD in adults has not yet been tested in Portugal and overall there is a gap in the literature regarding the role of partners in iCBT for SAD. The study will contribute to increase accessibility to therapy (and better mental health) by promoting online evidence-based therapies. Plus, it will help to better understand how relationship components are affected and affect clinical symptoms and their progression within receiving treatment.

Interventions

  • Behavioral PORTiSOFIE
    This treatment is based on the Clark and Wells model of social phobia, and it is constituted by 9 modules: 1. Introduction of the program and overview of social anxiety disorder and symptoms 2. Negative automatic thoughts 3. Challenging negative automatic thoughts 4. Behavioral experiments 5. Exposure 6. Exposure and self-focus attention 7. Exposure and get closer to fears 8. Social skill training 9. Maintenance plan

Primary outcome measures

  • Liebowitz Social Anxiety Scale for Adults (LSAS) [Time frame: through study completion, an average of 1 year]
  • Social Phobia Inventory (SPIN) [Time frame: through study completion, an average of 1 year]
  • Global Measure of Relationship Satisfaction (GMREL) [Time frame: through study completion, an average of 1 year]
  • Global Measure of Sexual Satisfaction (GMSEX) [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (4)
  • Revised Dyadic Adjustment Scale (RDAS) [Time frame: through study completion, an average of 1 year]
  • Inclusion of Other in the Self Scale (IOS) [Time frame: through study completion, an average of 1 year]
  • Difficulties in Interpersonal Emotion Regulation (DIRE) [Time frame: through study completion, an average of 1 year]
  • Personal Assessment of Intimacy in Relationships (PAIR) [Time frame: through study completion, an average of 1 year]

Eligibility criteria

Inclusion Criteria for participants:

  • Scores on the screening questionnaires indicating at least moderate levels of social anxiety.
  • Age 18 years or over
  • Fluency in Portuguese
  • Access to a device with internet
  • Be in a monogamous amorous relationship (regardless of sexual orientation)
  • Not be receiving any ongoing treatment for social anxiety (e.g., stable antidepressants).

Inclusion Criteria for partners:

  • Age 18 years or over
  • Fluency in Portuguese
  • Access to a device with internet.

Exclusion criteria

  • Self-reported severe psychiatric disorders such as psychosis or personality disorder.
  • Planned or ongoing medical treatments (e.g., surgery) and other personal circumstances that will interfere with the treatment (e.g., planned travel abroad).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Portugal · 1 center
  • Universidade Lusófona — Lisbon

Publications

  • Martins EM, Pascoal PM, Pereira M, Andersson G. Internet-based therapy for social anxiety in adults in Portugal (PORTiSOFIE) and its impact on sexual and relationship satisfaction: study protocol for a randomized controlled trial. Trials. 2025 Nov 6;26(1):476. doi: 10.1186/s13063-025-09103-2. PMID 41199378

Identifiers

NCT: NCT06767878 · 2024.03961.BD

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗