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Investigating Emotional Intelligence in Epilepsy

Investigating the Effect of a Program based on Emotional Intelligence components on Coping Strategies and Happiness in Epileptic Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180612040077N1
Enrollment
70
Registered
2018-08-01
Start date
2018-06-11
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Epilepsy. Epilepsy and recurrent seizures

Interventions

Intervention 1: Intervention group: Intervention in the experimental group was implemented as Emotional Intelligence Training Program in 8 sessions of 90 minutes over a period of 8 weeks (one session

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients at this Center have a Medical Record with Diagnosis of Grandmal Epilepsy and at least six months have passed since the onset of their Illness Able to Communicate They are aware of their Illness and are Interested in Participating in the Study Having the Physical and Mental Ability to Participate in the Study Patients are Selected from People aged 18 to 60 years The Absence of Cognitive Impairments and the Absence of other Mental or Physical Illnesses confirmed by the Physician and according to the Medical Records of the People under Study Having the Ability to Read and Write Not Participating in other Psychotherapy Programs during the Study No Drug Addiction and Psychotropic Substance Lack of Pregnancy Power and Possibility of Using the Sorosh Program No major Stress for the Person during the last month or during the Session

Exclusion criteria

Exclusion criteria: Unwillingness to Continue to Participate in the Study The Absence of a Patient in two Consecutive Sessions of Interventional Training Sessions for any Reason Make any Physical or Psychological Damage to the People who are not Able to Attend the Meetings

Design outcomes

Primary

MeasureTime frame
Coping Strategies. Timepoint: Before, Immediately, One month after the intervention. Method of measurement: Andler & Parker Coping Strategies Questionnaire.;Happiness. Timepoint: Before, Immediately, One month after the intervention. Method of measurement: Oxford Happiness Test Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNiloufar Hajisabbagh

Esfahan University of Medical Sciences

niloufar.hajisabbagh@gmail.com+98 31 3661 6759

Outcome results

None listed

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