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Investigating the effectiveness of neurofeedback on rumination and cognitive avoidance of people with obsessive-compulsive disorder

The effectiveness of neurofeedback on rumination and cognitive avoidance of people with obsessive-compulsive disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230526058295N1
Enrollment
30
Registered
2023-09-02
Start date
2023-09-06
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

People with obsessive compulsive disorder.

Interventions

Intervention group: Intervention group: 15 people will be assigned to the experimental group (related to neurofeedback exercises), 15 people will be assigned to the control group. The experimental gro

Sponsors

Rahnemon clinic
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: The selected people are willing and interested in participating in the study They Have obtained a minimum score of 16 from the 1986 Yale-Brown Obsession compulsion Questionnaire

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reducing post-test rumination and cognitive avoidance. Timepoint: Before the start of the intervention and two months after the start of the intervention. Method of measurement: Nolen, Hoeksma and Maro (1993) rumination questionnaire and Sexton and Dagas (2004) cognitive avoidance questionnaire in the pre-test and post-test stages.

Secondary

MeasureTime frame
Reducing the symptoms of obsessive-compulsive disorder. Timepoint: Two months after the start of the intervention. Method of measurement: Yale Brown Questionnaire (1986), Nolen, Hoeksma and Maro's Rumination Questionnaire (1993) and Sexton and Dagas Cognitive Avoidance Questionnaire (2004).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElahe azizi

Rahnemon clinic

e.azizi1998@gmail.com+98 933 490 8016

Outcome results

None listed

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