Evaluation of the effectiveness of neurofeedback therapy in patients with mild traumatic brain injury

Investigating the effectiveness of neurofeedback treatment on quality of life and functional attention in patients with mild brain trauma in two control and intervention groups.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230717058819N1

Enrollment

Registered

2023-10-14

Start date

2023-10-22

Completion date

Unknown

Last updated

2023-11-13

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

Conditions

mild traumatic brain injury. Concussion

Interventions

Intervention 1: Intervention group: 20 sessions neurofeedback. Intervention 2: Control group: 5 weeks without intervention.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients' Glasgow Coma Scale (GCS) should be between 13 and 15 at the time of admission to the emergency department. Patients should be between 18 and 60 years old. Patients who have at least a diploma

Exclusion criteria

Exclusion criteria: Patients who have a history of related diseases, mental disorders or substance abuse Patients who have experience of neurofeedback treatment. Patients who have been traumatized for more than six weeks

Design outcomes

Primary

Measure	Time frame
Quality of Life (SF-36). Timepoint: Before intervention & Five weeks after intervention. Method of measurement: Quality of Life Questionnaire (SF-36).;Continuous Attention Network. Timepoint: Before intervention & Five weeks after intervention. Method of measurement: Attention Network Task.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAdel Parvizi-Fard

Artesh University of Medical Sciences

adel.p1372@gmail.com+98 83 3433 0349

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026