Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06422442 · ClinicalTrials.gov registry record · NA

Information Processing Biases in Adults Who Stutter

A NA study of Stuttering, Adult, sponsored by University of Memphis.

Recruiting
Registry status
NA
Development phase
80
Enrollment target
1
Study location

NCT06422442: Recruiting NA study of Stuttering, Adult, sponsored by University of Memphis.

NCT06422442 is a NA study of Stuttering, Adult that is actively recruiting participants, run by University of Memphis. The registered enrollment target is 80 participants, below the 653-participant average among 5 other Stuttering, Adult trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06422442, a NA study of Stuttering, Adult, is actively recruiting participants, sponsored by University of Memphis.

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

Study Summary

The goal of this clinical trial is to examine whether stuttering is associated with a tendency to attend more quickly or for longer durations to threat-related information in the environment (threat-related attention bias). The main questions it aims to answer are: Do adults who stutter, relative to adults who do not stutter, attend to threat-related stimuli more than neutral information? Are attentional biases observed across different types of threat or are they specific to threats related to stuttering experiences? Do measures of attention bias explain individual differences in psychological reactions among adults who stutter?

Conditions Studied

Interventions

  • BEHAVIORAL Threat-related stimulus exposure

Study Locations (1)

Tennessee

  • University of Memphis - Memphis

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2023-09-11
Est. Completion 2026-06-30
Phase NA
University of Memphis

35 total trials

What NCT06422442 shows while recruiting

NCT06422442 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 653-participant average among 5 other Stuttering, Adult trials with a reported enrollment target (88% lower).

The record links to 1 condition, with Stuttering, Adult appearing as the primary indexed condition, and to 1 intervention - of which Threat-related stimulus exposure is the first listed.

NCT06422442 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT06422442 about?

NCT06422442 is a clinical study titled "Information Processing Biases in Adults Who Stutter". The goal of this clinical trial is to examine whether stuttering is associated with a tendency to attend more quickly or for longer durations to threat-related information in the environment (threat-related attention bias). The main questions it aims to answer are: Do adults who stutter, relative t...

What is the current status of trial NCT06422442?

This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2023-09-11. Estimated completion is 2026-06-30.

What conditions does trial NCT06422442 study?

This clinical trial studies the following conditions: Stuttering, Adult.

What interventions are being tested in trial NCT06422442?

The interventions under investigation include: Threat-related stimulus exposure (BEHAVIORAL).

Who is sponsoring clinical trial NCT06422442?

This trial is sponsored by University of Memphis, which has 35 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06422442 being conducted?

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

Similar trials for Stuttering, Adult

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01243931 · 80 participants · NA

    Optical Coherence Tomography Guided Transepithelial Phototherapeutic Keratectomy

  • NCT01659203 · 80 participants · Phase 1

    Proton or Photon RT for Retroperitoneal Sarcomas

  • NCT01803451 · 80 participants · Early Phase 1

    Glucagon-like Peptide 1, Glucose Metabolism and Gastric Bypass

  • NCT01964859 · 80 participants · Phase 2

    Feasibility Study for Fibroblast Autologous Skin Grafts

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06422442, the US trial registry maintained by the National Library of Medicine. NCT06422442 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.