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TFCBT and eTFCBT for Traumatic Stress Disorders

N/A
Waitlist Available
Research Sponsored by Medical University of South Carolina
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 3, 6, 9, 12 months post baseline
Awards & highlights

Study Summary

This trial will test whether a tablet-based toolkit can improve mental health outcomes for children aged 8-16 who have symptoms of PTSD.

Eligible Conditions
  • Post-Traumatic Stress Disorder
  • Technology
  • Child Abuse

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 3, 6, 9, 12 months post baseline
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 3, 6, 9, 12 months post baseline for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Child Involvement Ratings Scale
Provider Treatment Fidelity
Secondary outcome measures
Acceptability, Appropriateness and Feasibility Measure (
Brief Problems Monitor (BPM)
Burnout Measure
+16 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Tablet-Facilitated TF-CBTExperimental Treatment1 Intervention
Standard treatment with the addition of in-treatment/session iPad activities
Group II: Treatment as usualActive Control1 Intervention
Trauma Focused Cognitive Behavioral Therapy
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
eTFCBT
2018
N/A
~260

Find a Location

Who is running the clinical trial?

Medical University of South CarolinaLead Sponsor
932 Previous Clinical Trials
7,394,001 Total Patients Enrolled

Media Library

TFCBT 2023 Treatment Timeline for Medical Study. Trial Name: NCT03305458 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What primary aims are being tested through the course of this medical experiment?

"The objective of this trial, which is expected to last 12-20 weeks per participant, will be the evaluation of Treatment Fidelity. Secondary outcomes are Working Alliance Inventory (WAI-short form), Brief Problems Monitor (BPM) and The Kessler 6; WAI being a 12-item measure of parent/therapist alliance on a 7 point scale, BPM as 19 item measure for emotional & behavioral functioning in children similar to Child Behavior Checklist, and Kessler 6 as widely used 6-item marker of general distress."

Answered by AI

Is there still eligibility to join this research endeavor?

"This trial is open to 360 children and adolescents between the ages of 8-16 who have access to technology. In addition, participants must have endured at least one traumatic event (including sexual/physical assault, seen violence, experienced a disaster or serious accident) as well as present symptoms from each PTSD symptom cluster (repetitive memories, evasion tactics, heightened awareness)."

Answered by AI

How many individuals can participate in the trial at one time?

"Affirmative. Clinicaltrials.gov confirms that this research project, which was initially advertised on October 1st 2018, is actively enrolling patients. A total of 360 participants will be admitted to the trial at a single site."

Answered by AI

Are any openings available for potential participants in this experiment?

"According to the information hosted on clinicaltrials.gov, this trial is actively recruiting participants with a start date of October 1st 2018 and an update made on September 20th 2022."

Answered by AI

Could seniors aged 65 and over participate in this trial?

"According to the instructions, only individuals between 8 and 16 years old are considered suitable for this trial. Furthermore, there are 53 trials targeting those under 18 and 345 specifically designed for seniors above 65."

Answered by AI
~40 spots leftby Apr 2025