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The effect of Neurofeedback self-regulating training in patients with PTSD

Clinical study on the effect of Neurofeedback self-regulating training in patients with PTSD: A Randomized, Waitlist-control Clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003271
Enrollment
46
Registered
2018-10-18
Start date
2019-05-02
Completion date
Unknown
Last updated
2021-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : As a kind of manipulative condition training, it is a feedback training in which the subject learns reinforcement and compensation while monitoring their brain waves by themselves. In ord

Sponsors

Wonkwang University Sanbon Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) 20 ~ 55 year old male and female adults 2) Those diagnosed with PTSD according to the SCID-5 (Structured Clinical Interview for DSM-5) criteria 3) Trauma occurred more than 6 months 4) Those who voluntarily agreed to participate after receiving explanation of the purpose and process of this clinical trial

Exclusion criteria

Exclusion criteria: 1) Those with a severef mental illness    ? Who has a recent or past delusion or hallucination    ? At least one manic episode appears    ? Who has a alcohol abuse or dependency history    ? Those who are at risk of suicide 2) If it is necessary to continuously administer a substance that is thought to have an effect on symptom induction, excluding concomitant medication 3) Those who have serious problems with congenital diseases, central nervous system, peripheral nervous system diseases, endocrine diseases, immunological diseases, heart, liver and kidney system 4) Those who are pregnant or lactating 5) Those who have participated in other clinical studies for the past month or are currently participating in other clinical studies. 6) Those who are deemed difficult to carry out the clinical trial by clinical reserarcher

Design outcomes

Primary

MeasureTime frame
The Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5-K)

Secondary

MeasureTime frame
Impact of Event Scale-Revised (IES-R-K);The Clinical Global Impression–Improvement scale (CGI-I);Beck Anxiety Inventory (BAI);Beck Depression Inventoy (BDI);Insomnia severity index (ISI);Hwabyung Score;The Core Seven-Emotions Inventory Short Form (CSEI-S);Quantative encephalogram (QEEG);Mentalizing the Rooms of Mind (MRM);Economic analysis;Safety assessment

Countries

Korea, Republic of

Contacts

Public ContactHyung Won Kang

Wonkwang University Sanbon Hospital

onp21@hanmail.net+82-31-390-2763

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 18, 2026