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Not yet recruiting NCT06155565

Understanding Patient Engagement Trends in Anxiety Disorder Clinical Research

Observational Anxiety Disorder

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Anxiety Disorder. 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
United States
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

Investigating Patterns in Enrollment and Engagement Among Individuals Coping With Anxiety Disorder

Overview

Clinical trials, specifically focused on anxiety disorder, are crucial in assessing the safety and efficacy of new treatments. These trials serve as fundamental instruments in determining whether emerging medications outperform standard therapies, providing compelling evidence to support wider implementation. The main goal is to thoroughly scrutinize trial completion rates and voluntary withdrawals among this particular group of patients.

Primary outcome measures

  • Number of anxiety disorder patients who decide to enroll in a clinical research [Time frame: 3 months]
  • Rate of anxiety disorder patients who remain in clinical trial to trial completion [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Aged ≥ 18 years old
  • Diagnosis of anxiety disorder
  • Able to comprehend the investigational nature of the protocol and provide informed consent

Exclusion criteria

  • Female patients who are currently pregnant or nursing
  • Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
  • Inability to perform regular electronic reporting

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

Healthy volunteers: No

Study design

Observational model
Case-crossover

Study locations

United States · 1 center
  • Power Life Sciences — San Francisco

Publications

  • Szuhany KL, Simon NM. Anxiety Disorders: A Review. JAMA. 2022 Dec 27;328(24):2431-2445. doi: 10.1001/jama.2022.22744. PMID 36573969
  • Yee A, Ng CG, Seng LH. Vortioxetine Treatment for Anxiety Disorder: A Meta-Analysis Study. Curr Drug Targets. 2018;19(12):1412-1423. doi: 10.2174/1389450118666171117131151. PMID 29149828
  • Liao J, Kang J, Li F, Li Q, Wang J, Tang Q, Mao N, Li S, Xie X. A cross-sectional study on the association of anxiety and depression with the disease activity of systemic lupus erythematosus. BMC Psychiatry. 2022 Sep 5;22(1):591. doi: 10.1186/s12888-022-04236-z. PMID 36064377

Identifiers

NCT: NCT06155565 · 65829005

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗