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Proactive Thought Control for Social Anxiety Relief (PTC - SA)

15 de julho de 2026 atualizado por: Saba Ahmad, GIFT University

The Effectiveness of Proactive Thought Control in Modification of Negative Core Beliefs and Cognitive Biases in Individual With Social Anxiety: A Pilot RCT Study

This study examines whether a proactive thought control intervention can reduce negative core beliefs, cognitive biases, and anxiety symptoms in university students with social anxiety. Participants with elevated social anxiety (screened via the Liebowitz Social Anxiety Scale) are randomly assigned to either a proactive thought control group or a reactive control group. Both groups complete two computerized tasks - a Free Association Task and a Sentence Completion Task - across 180 trials. The proactive group is trained to generate only positive or neutral associations to socially threatening cues and receives real-time AI-powered sentiment feedback, while the reactive group responds freely without sentiment-based guidance. Outcomes including negative core beliefs, interpretation bias, attentional bias, state anxiety, and trait anxiety are assessed before and after the intervention using standardized measures (CBQ, WSAP, Dot Probe Task, STAI). The study uses a parallel-group randomized controlled trial design with repeated measures and aims to establish preliminary effect size estimates for future, larger-scale trials.

Visão geral do estudo

Descrição detalhada

Background and Rationale Social anxiety disorder (SAD) is characterized by intense fear of negative evaluation in social situations, leading to significant avoidance and distress. Cognitive models of SAD emphasize the role of negative core beliefs (e.g., beliefs about being inferior or unacceptable to others) and cognitive biases - particularly interpretation bias and attentional bias toward threat - in the maintenance of the disorder. While cognitive bias modification (CBM) approaches have shown promise, most are reactive in nature, modifying biases after they arise. Proactive cognitive control, by contrast, involves the sustained, goal-directed maintenance of positive or neutral mental sets before threatening stimuli are encountered. This study tests whether a proactive approach to thought control, delivered through modified free association and sentence completion paradigms, can more effectively shift core beliefs and cognitive biases compared to a reactive control condition.

Study Design This is a parallel-group randomized controlled trial (RCT) with a repeated-measures (pre-post) design. Participants are randomly assigned using the fishbowl block randomization technique to either: (1) the Proactive Thought Control group, or (2) the Reactive Control group (active sham condition). Counterbalancing is applied to the order of stimuli in the WSAP and Dot Probe Task to control for practice effects.

Participants Participants are university students aged 18-24 years, recruited via purposive sampling using the Liebowitz Social Anxiety Scale - Self Report (LSAS-SR). Individuals scoring above 30 on the LSAS-SR are eligible. Exclusion criteria include current psychological treatment, psychiatric or medical comorbidities, and medication use. Of 204 initially screened, 149 met the LSAS cutoff; 54 were enrolled and randomized. Final analyses include 37-39 participants who completed both pre- and post-assessments. As a pilot trial, this sample size is consistent with recommended ranges of 15-30 participants per group for feasibility and preliminary effect size estimation.

Measures

Pre- and post-intervention assessments include:

Core Belief Questionnaire (CBQ): Measures negative core beliefs about self and others in social anxiety (trait and other subscales used).

Spielberger State-Trait Anxiety Inventory - Short Form (STAI): Assesses state and trait anxiety (5 items each; 4-point Likert scale).

Word Sentence Association Paradigm (WSAP): Computerized task measuring interpretation bias; participants judge relatedness of threatening/benign word-sentence pairs. Bias scored as proportion of threatening endorsements.

Dot Probe Task: Computerized task measuring attentional bias toward threat using reaction time differences (Attentional Bias Index = mean RT threat-incongruent minus mean RT threat-congruent trials).

Screening measures include the LSAS-SR and DASS-12 (for baseline distress comparability).

Intervention The intervention comprises 180 trials divided into six blocks (framed as "game levels"): three blocks of Free Association Task (FAT) and three blocks of Sentence Completion Task (SCT). Each block contains 25 socially threatening stimuli and 5 positive/neutral stimuli, presented in randomized order.

Free Association Task (FAT): Participants see a single threatening or neutral word cue and respond with the first word that comes to mind. The proactive group is instructed to produce only positive or neutral single-word associations and cannot advance until doing so. The reactive group responds freely.

Sentence Completion Task (SCT): Participants complete unfinished sentence stems (e.g., "They stared, and I felt ___"). The proactive group must provide positive or neutral completions; the reactive group responds without restriction.

A real-time AI feedback system powered by DistilBERT-base-uncased-finetuned-SST-2-English (a lightweight transformer model fine-tuned for binary English sentiment classification) evaluates responses. Both groups receive quality-based feedback (for repetitions, spelling errors, and invalid inputs). The proactive group additionally receives sentiment-based reinforcement: +2 points and "Correct" feedback for positive/neutral responses, and corrective guidance for negative responses. The reactive group receives no sentiment feedback. This gamified point system reinforces goal-directed positive thinking in the proactive group.

Procedure Participants are recruited in-person (paper-based classroom administration) and online (Google Form). Following informed consent and LSAS/DASS screening, eligible participants complete pre-assessment (CBQ, STAI, WSAP, Dot Probe Task) via OpenSesame software, then complete the intervention tasks, followed immediately by post-assessment using the same battery.

Data Analysis Data cleaning and scoring are conducted using Excel and R (packages: jsonlite, readxl, dplyr, tidyr, stringr, writexl). Statistical analyses are conducted in SPSS and include: chi-square for attrition analysis; descriptive statistics for demographics; Mixed ANOVA for main and interaction effects (Group × Time); paired-sample t-tests for within-group pre-post comparisons; independent-sample t-tests for between-group comparisons; and ANCOVA to isolate intervention effects from baseline differences.

Tipo de estudo

Intervencional

Inscrição (Real)

54

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Punjab Province
      • Gujranwala, Punjab Province, Paquistão, 52250
        • GIFT University

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria

  • being 18-24 years old
  • not taking any additional psychological treatments during the trial
  • If taking medication for depression or anxiety, the dosage had to remain consistent for one month before the start of therapy.
  • Cut off score above 30 in LSAS
  • Consent to participate in the study and complete all tasks.
  • Proficiency in English
  • Regularly computer user Exclusion Criteria
  • Age below 18 or above 24 years
  • Currently receiving psychological treatment
  • Failure to provide consent or complete the study tasks
  • Have any other medical condition
  • Have any other psychiatric condition
  • Taking medicineInclusion Criteria:

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Proactive Thought Control
Participants in this arm completed a modified Free Association Task (FAT) and Sentence Completion Task (SCT) across 180 trials (6 blocks of 30). They were instructed to generate only positive or neutral single-word responses to socially threatening cues and could not advance within a trial until doing so. Real-time AI-powered sentiment feedback (DistilBERT) reinforced positive/neutral responses with "+2 Score" and corrective guidance for negative responses. A gamified points system sustained engagement. Pre- and post-assessments included the CBQ, STAI, WSAP, and Dot Probe Task.
A computerized behavioral intervention delivered across 180 trials in six blocks. The first three blocks use a Free Association Task (FAT), where participants respond to single threatening or neutral word cues. The last three blocks use a Sentence Completion Task (SCT), where participants complete socially threatening or neutral sentence stems. Participants in the proactive group must generate positive or neutral single-word responses and cannot advance until doing so. Real-time sentiment feedback is delivered via DistilBERT (an AI language model), awarding +2 points for positive/neutral responses and providing corrective guidance for negative ones. The reactive control group completes identical tasks but responds freely, receiving only neutral quality-based feedback without sentiment reinforcement. Both groups receive feedback for repeated, misspelled, or invalid entries. Each block contains 25 threatening and 5 positive/neutral stimuli presented in randomized order.
Comparador Ativo: Reactive Thought Control
Participants in this arm completed the same Free Association Task (FAT) and Sentence Completion Task (SCT) across 180 trials (6 blocks of 30) as the experimental group, but responded freely without any restriction on response valence. They received only neutral quality-based feedback (e.g., for repeated, misspelled, or invalid entries) with no sentiment-based reinforcement or corrective guidance. This active sham condition controlled for task engagement, the Hawthorne effect, and demand characteristics. Pre- and post-assessments were identical to those of the experimental arm.
A computerized behavioral sham condition delivered across 180 trials in six blocks, identical in structure to the experimental intervention. The first three blocks use a Free Association Task (FAT) and the last three use a Sentence Completion Task (SCT), both involving socially threatening and neutral stimuli. Participants respond freely with any single-word association without restriction on response valence. No sentiment-based feedback or scoring is provided. Participants receive only neutral quality-based feedback for repeated, misspelled, or invalid entries. This condition controls for nonspecific factors including task engagement, time-on-task, the Hawthorne effect, and demand characteristics, while isolating the active ingredient of proactive sentiment-directed training present in the experimental arm.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Core Beliefs: Change in Negative Core Beliefs as Measured by the Core Belief Questionnaire (CBQ)
Prazo: Baseline (pre-intervention) and immediately after intervention completion (post-intervention)
The Core Belief Questionnaire (CBQ; Wong et al., 2017) measures negative core beliefs in socially anxious individuals across three versions: trait (beliefs about self), contingent (beliefs about self when negatively evaluated), and other (beliefs about others). Each scale contains 17 items rated on a 6-point Likert scale (1 = strongly disbelieve to 6 = strongly believe). Total scores range from 17 to 102, with higher scores indicating stronger negative core beliefs. In this study, the trait and other subscales are used. Change scores from pre- to post-intervention are compared between the proactive thought control group and the reactive control group.
Baseline (pre-intervention) and immediately after intervention completion (post-intervention)
Interpretation Biases: Change in Interpretation Bias as Measured by the Word Sentence Association Paradigm (WSAP)
Prazo: Baseline (pre-intervention) and immediately after intervention completion (post-intervention)
The WSAP (Beard & Amir, 2009) is a computerized task measuring interpretation bias toward threatening versus benign interpretations of ambiguous social scenarios. Each trial presents a word cue followed by an ambiguous sentence; participants judge relatedness by pressing Y or N. Bias is scored as the proportion of trials in which participants endorse threatening word-sentence pairings. Higher proportions indicate stronger negative interpretation bias. The task includes 30 trials with threatening and benign word-sentence pairs presented in randomized, counterbalanced order across pre- and post-assessments.
Baseline (pre-intervention) and immediately after intervention completion (post-intervention)
Attentional Biases: Change in Attentional Bias as Measured by the Dot Probe Task
Prazo: Baseline (pre-intervention) and immediately after intervention completion (post-intervention)
The Dot Probe Task (MacLeod et al., 1986) measures attentional bias toward threatening stimuli using reaction times. Each trial presents a threatening and a neutral word simultaneously; a probe then replaces one stimulus. The Attentional Bias Index (ABI) is calculated as: mean RT on threat-incongruent trials minus mean RT on threat-congruent trials. Positive ABI scores indicate vigilance toward threat; negative scores indicate avoidance; scores near zero indicate no bias. Trials with RTs below 200 ms or above 1500 ms and incorrect responses are excluded. The task includes 30 trials in counterbalanced, randomized order across assessments.
Baseline (pre-intervention) and immediately after intervention completion (post-intervention)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
State Trait Anxiety:Change in State-Trait Anxiety as Measured by the STAI - Short Form (STAI-State Subscale)
Prazo: Baseline (pre-intervention) and immediately after intervention completion (post-intervention)

The short-form State-Trait Anxiety Inventory (Zsido et al., 2020) state subscale consists of 5 items assessing temporary anxiety symptoms such as tension and apprehension. Items are rated on a 4-point Likert scale (0 = not at all to 3 = very much so), with total scores ranging from 5 to 20. Higher scores indicate greater state anxiety. Change from pre- to post-intervention is compared between groups.

The short-form State-Trait Anxiety Inventory (Zsido et al., 2020) trait subscale consists of 5 items assessing stable individual differences in anxiety proneness. Items are rated on a 4-point Likert scale (0 = not at all to 3 = very much so), with total scores ranging from 5 to 20. Higher scores reflect greater trait anxiety. Change from pre- to post-intervention is compared between the proactive thought control and reactive control groups.

Baseline (pre-intervention) and immediately after intervention completion (post-intervention)

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Baseline Depression, Anxiety, and Stress Levels as Measured by the DASS-12
Prazo: Screening only
The DASS-12 (Monteiro et al., 2023) is a 12-item self-report measure with three 4-item subscales assessing depression, anxiety, and stress over the past week. Items are rated on a 4-point Likert scale (0 = did not apply at all to 3 = applied most of the time). It is used at screening only to verify baseline equivalence between groups and to control for the influence of general distress on intervention outcomes. It is not used as a primary or secondary outcome measure.
Screening only

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Publicações e links úteis

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Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

20 de abril de 2025

Conclusão Primária (Real)

30 de maio de 2025

Conclusão do estudo (Real)

30 de junho de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

25 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

25 de abril de 2026

Primeira postagem (Real)

1 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

16 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

15 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • GIFT/HSS/2025/PSY/1025
  • self funded (Outro identificador: Faculty of Dentistry, Ain Shams University Research Ethics Committee (FDASU-REC))

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

Plan Description:

De-identified individual participant data (IPD) underlying the primary and secondary outcome analyses will be shared, including pre- and post-intervention scores on the Core Belief Questionnaire (CBQ), Word Sentence Association Paradigm (WSAP), Dot Probe Task, and State-Trait Anxiety Inventory (STAI). Raw reaction time data from the WSAP and Dot Probe Task, demographic data, and group assignment variables will also be made available. Data will be de-identified in accordance with standard anonymization procedures to protect participant confidentiality. Screening data (SCID, LSAS-SR and DASS-12) will be shared at aggregate level only.

Prazo de Compartilhamento de IPD

IPD and supporting information will be available beginning 6 months after publication of primary study findings and will remain accessible for a minimum of 5 years following initial data sharing.

Critérios de acesso de compartilhamento IPD

De-identified IPD will be available to qualified academic researchers for non-commercial research purposes. Requestors must submit a brief research proposal describing the intended use of the data, confirm compliance with applicable ethical and data protection regulations, and sign a data use agreement. Requests will be reviewed by the principal investigator. Data will be shared via a secure file transfer or repository link upon approval.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • CIF
  • ANALYTIC_CODE

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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