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NCT04895995 · ClinicalTrials.gov registry record · NA

Initial Assessment of the Feasibility and Efficacy of a Scalable Digital CBT for Generalized Anxiety and Associated Health Behaviors in a Cardiovascular Disease Population

A NA study of Anxiety and Cardiovascular Diseases, sponsored by Boston University Charles River Campus.

Recruiting
Registry status
NA
Development phase
95
Enrollment target
1
Study location

NCT04895995 is a NA study of Anxiety and Cardiovascular Diseases that is actively recruiting participants, run by Boston University Charles River Campus. The registered enrollment target is 95 participants, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (78% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04895995, a NA study of Anxiety and Cardiovascular Diseases, is actively recruiting participants, sponsored by Boston University Charles River Campus.

RECRUITING
Registry status
NA
Development phase
95 participants
Enrollment target
1
Study location

Study Summary

The treatment of generalized anxiety disorder (GAD) in an accessible manner represents an unmet need for those with cardiovascular disease (CVD), given that patients with CVD experience numerous barriers for in-person treatment engagement. The research plan for the proposed pilot project will entail: (1) open study of the acceptability of the digital intervention (N=5), followed by (2) recruitment and randomization of 90 individuals with a history of acute CVD events and clinical levels of GAD symptoms to dCBT or a waitlist (Control) condition, using a 1.5:1 allocation (dCBT:Control).

Interventions

  • BEHAVIORAL Daylight dCBT Application

Study Locations (1)

Massachusetts

  • Boston University - Boston

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2022-02-02
Est. Completion 2026-03-15
Phase NA

What the Registry Record Tells You About NCT04895995

The ClinicalTrials.gov registry entry for NCT04895995 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 95 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (78% lower). The listed sponsor is Boston University Charles River Campus, which has 104 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Anxiety appearing as the primary indexed condition, and to 1 intervention - of which Daylight dCBT Application is the first listed.

NCT04895995 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04895995 about?

NCT04895995 is a clinical study titled "Initial Assessment of the Feasibility and Efficacy of a Scalable Digital CBT for Generalized Anxiety and Associated Health Behaviors in a Cardiovascular Disease Population". The treatment of generalized anxiety disorder (GAD) in an accessible manner represents an unmet need for those with cardiovascular disease (CVD), given that patients with CVD experience numerous barriers for in-person treatment engagement. The research plan for the proposed pilot project will entail...

What is the current status of trial NCT04895995?

This trial is currently recruiting. It is a NA study. The enrollment target is 95 participants. The study started on 2022-02-02. Estimated completion is 2026-03-15.

What conditions does trial NCT04895995 study?

This clinical trial studies the following conditions: Anxiety, Cardiovascular Diseases, Anxiety Disorders, Health Behavior.

What interventions are being tested in trial NCT04895995?

The interventions under investigation include: Daylight dCBT Application (BEHAVIORAL).

Who is sponsoring clinical trial NCT04895995?

This trial is sponsored by Boston University Charles River Campus, which has 104 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04895995 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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