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Clinical Trials/NCT05172427
NCT05172427
Unknown
N/A

Acceptability/Feasibility Testing of an Intervention Targeting Intolerance of Uncertainty

Ohio University1 site in 1 country45 target enrollmentSeptember 15, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Generalized Anxiety Disorder
Sponsor
Ohio University
Enrollment
45
Locations
1
Primary Endpoint
Feasibility of service
Last Updated
4 years ago

Overview

Brief Summary

Anxiety disorders are prominent mental health burdens, affecting roughly 1 in 5 adults annually, and a third of individuals over the course of their life. These disorders are also impairing to individuals, with 23% of individuals with anxiety disorders describing their impairment as serious. Given the public health impact, it is crucial that interventions are designed to alleviate symptoms of anxiety, through reducing risk factors that predispose individuals to develop anxiety. One approach to do this is to develop brief interventions that could be administered virtually, which can then be supplemented using ecological momentary intervention (EMI) to reduce risk factors for anxiety disorders. In contrast to targeting more distant risk factors, targeting more direct risk factors, such as intolerance of uncertainty, could be used in the prevention and treatment of anxiety disorders.

Detailed Description

Anxiety disorders have been estimated to impact roughly 1 in 5 (19%) adults in the United States over the past year, and almost a third (31%) of adults in the United States over the course of their life. Further, these disorders are impairing to individuals; 23% of individuals with anxiety disorders describing their impairment as serious. Given this public health impact, it is crucial, that interventions are designed to alleviate symptoms of anxiety, or to reduce risk factors that may predispose individuals to develop anxiety. Further, it is expected that the COVID-19 will have long-lasting impacts on mental concerns worldwide. With these concerns come new opportunities to improve mental health care, through ultra-brief, self-paced, web-based interventions. These interventions are ideal to increase access to care given their high dissemination value and low cost. Building on prior experimental and intervention work conducted by Dr. Allan, we aim to conduct pilot testing of an ultra-brief, CBT-informed intervention targeting intolerance of uncertainty, or an extreme aversion to and fear of uncertainty. Intolerance of uncertainty is an ideal construct to target in a broad web-based intervention given theoretical and empirical links between intolerance of uncertainty and a broad spectrum of anxiety and related disorders. Theoretically, intolerance of uncertainty amplifies the experience of stress and anxiety causing people to engage in maladaptive cognitive (e.g., worry) and behavioral (e.g., checking, avoidance) strategies to reduce distress, preventing an opportunity to habituate to the uncertainty. Empirically, a recent meta-analysis reported effect sizes (ds) ranging from .4 to .6 across generalized anxiety disorder, major depression, obsessive compulsive disorder, social anxiety disorder, panic disorder and agoraphobia, and eating disorders. Other studies have implicated intolerance of uncertainty in posttraumatic stress disorder as well as suicidal thought and behavior. More recent evidence has demonstrated that intolerance of uncertainty is not only a "fundamental fear" underlying anxiety disorder etiology but has also been implicated in a host of other mental health problems, including substance use. We recently examined the impact of intolerance of uncertainty on anxiety and depression during the COVID-19 pandemic over three months and found intolerance of uncertainty was concurrently associated with and significantly predictive of symptoms of generalized anxiety disorder and depression. Therefore, not only is there strong theoretical and empirical support for intolerance of uncertainty as a transdiagnostic risk factor for anxiety and related conditions, but there is also evidence that supports intolerance of uncertainty as particularly relevant to the current environmental conditions due to COVID-19. To date, we have conducted the only pilot RCT of a CBT-based intervention (clinicaltrials.gov NCT04199884). In a sample of 84 participants with elevated intolerance of uncertainty during their screening appointment, we compared a researcher-facilitated Intolerance of Uncertainty Treatment (IUT) to a time-matched healthy living control condition. IUT contains psychoeducation, challenging negative automatic thoughts regarding uncertainty through "mythbusting" exercises, and designing behavioral experiments to challenge these negative automatic thoughts. In this study, significant, medium effect size differences (d = .46) emerged between IUT and the control condition, but not until the month 1 follow-up. In addition, reductions in intolerance of uncertainty served as indirect effects from treatment condition to anxiety and depression symptoms. Further, most people found the intervention easy to understand, helpful, and applicable to their daily lives. Building on this prior work, we plan to adapt the existing ultra-brief intolerance of uncertainty intervention to be disseminated via a web-based computerized platform. Given the flexibility afforded via this digital platform, we also propose to include ecological momentary intervention (EMI) to enhance learning through the application of critical interventions skills as needed. EMI is ideal for these brief interventions as it allows for participants to gain the much-needed practice of challenging negative automatic thoughts and completing behavioral experiments critical to internalizing the skills and strategies taught during the intervention. Similar augmentations to brief interventions for stress, generalized anxiety disorder, and panic disorder (d = .5) have been successful in enhancing intervention effects (i.e., an additional d of .4 to .6), further underscoring the promise of including EMI to optimize outcomes. The goals specific to this project are to 1) engage stakeholders in the design of an ultra-brief intolerance of uncertainty intervention (Enhanced Intolerance of Uncertainty Treatment \[E-IUT\]) and 2) to conduct a pilot trial to evaluate the acceptability, feasibility, and preliminary effect size estimates of E-IUT, in support of a larger fully powered test of E-IUT.

Registry
clinicaltrials.gov
Start Date
September 15, 2021
End Date
December 31, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nicholas Allan

Assistant Professor of Clinical Psychology

Ohio University

Eligibility Criteria

Inclusion Criteria

  • Elevated GAD symptoms (i.e., GAD-7 scores greater than or equal to 10)
  • Elevated IU symptoms (i.e., IUS-12 scores greater than or equal to 28)
  • Access to a device with internet connection

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Feasibility of service

Time Frame: 14-day EMA/EMI

Feasibility will also be determined based on response rates for EMA/EMI. If 80% of participants respond to 80% of the EMA prompts, this will be considered a feasible means of service delivery

Client Satisfaction Questionnaire-8

Time Frame: One month follow up

The CSQ-8 is a 8-item self-report scale that assesses client satisfaction with a particular intervention/program. The CSQ-8 is completed by rating satisfaction with services on a 1-4 Likert-type scale

Secondary Outcomes

  • PROMIS depression scale(One month follow up)
  • COVID-19 impact battery short-form (CIB-SF)(One month follow up)
  • Insomnia Severity Index (ISI)(One month follow up)
  • PROMIS anxiety scale(One month follow up)
  • Firearm ownership(One month follow up)
  • Oxford Covid-19 Vaccine Hesitancy Scale(One month follow up)
  • Drug Use Disorders Identification Test (DUDIT)(One month follow up)
  • Intolerance of Uncertainty-12(One month follow up)
  • PROMIS stress scale(One month follow up)
  • The Anxiety Depression Distress Inventory-27 (ADDI-27)(One month follow up)
  • Positive and Negative Affect Schedule-SF(One month follow up)
  • Alcohol Use Disorder Identification Test (AUDIT)(One month follow up)
  • COVID-19 contraction questions(One month follow up)
  • Penn State Worry Questionnaire (PSWQ)(One month follow up)
  • The Metacognition Questionnaire-30 (MCQ)(One month follow up)
  • EMA questions(14-day EMA/EMI period)
  • Perseverative Thought Questionnaire (PTQ)(One month follow up)
  • Ruminative Response Scale (RRS)(One month follow up)

Study Sites (1)

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