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Attention Control Training for PTSD in Children
Study Summary
This trial is testing whether attention control training can help people with PTSD.
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Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- You have experienced a traumatic event within the last month before starting the trial.You have severe symptoms of PTSD and have experienced a traumatic event that meets the study's criteria.
- Group 1: Attention Control Training
- Group 2: Comparison Task
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are minors within the age range of eligibility for this clinical research experiment?
"This clinical trial mandates that participants are aged between 7 and 15 years old, inclusive."
How many volunteers are engaged in this clinical experiment?
"Affirmative. The clinical trial's listing on clinicaltrials.gov verifies that the study is actively searching for individuals to participate. It was initially posted in November of 2017 and last updated in July of 2022, aiming to recruit 60 patients from one site."
Is this investigation currently looking for participants?
"As evidenced by the clinicaltrials.gov website, this trial is in need of volunteers and has been since its posting on November 20th 2017. Its most recent edit was made July 15th 2022."
To whom is this clinical trial accessible?
"This trial requires participants to be aged between 7 and 15, with a documented case of Post Traumatic Stress Disorder (PTSD). Approximately 60 people are required for this research."
Who else is applying?
What state do they live in?
How old are they?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
What questions have other patients asked about this trial?
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