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The effect of eye movement desensitization and reprocessing therapy on anxiety

The effectiveness of eye movement desensitization and reprocessing therapy on anxiety in undergraduate psychology students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250311065038N1
Enrollment
30
Registered
2025-04-20
Start date
2025-05-10
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Anxiety. Other anxiety disorders

Interventions

Intervention 1: Intervention group: The experimental group will undergo an eye movement desensitization and reprocessing (EMDR) therapy intervention. This intervention will be delivered over 8 weekly

Sponsors

Islamic Azad University, Semnan branch
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: Female undergraduate student in psychology (semesters 2 to 8). Age between 18 and 25 years at the time of study entry. Having a moderate to severe level of anxiety based on the Spielberger Anxiety Inventory score. Willingness and informed consent to participate in the research. Not receiving EMDR therapy in the past six months. Commitment to regular attendance at all treatment sessions and to complete pre- and post-tests.

Exclusion criteria

Exclusion criteria: Having a severe psychiatric disorder (such as psychosis, active bipolar disorder, schizophrenia, or borderline personality disorder) as clinically assessed. Unstable psychiatric medication use (start or change of medication within the last 6 weeks). History of severe brain injury or active seizures. Concurrent participation in other psychological or pharmacological treatments for anxiety at the time of the research. Drug or alcohol abuse within the last three months. Pregnancy or breastfeeding at the time of research. Unwillingness or inability to attend therapy sessions regularly and complete assessment procedures.

Design outcomes

Primary

MeasureTime frame
Anxiety. Timepoint: Before the start of the intervention and after completing 8 intervention sessions. Method of measurement: Spielberger Anxiety Inventory (1970).

Secondary

MeasureTime frame
Quality of Life. Timepoint: Before the start of the intervention and after completing 8 intervention sessions. Method of measurement: World Health Organization Quality of Life Questionnaire (1996).;Self-Efficacy Beliefs. Timepoint: Before the start of the intervention and after completing 8 intervention sessions. Method of measurement: General Self-Efficacy Scale by Scherer et al. (1982).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAtefeh Bidukhti

Islamic Azad University, Semnan Branch

ate_danesh1362@yahoo.com+98 23 3365 4045

Outcome results

None listed

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