Neuro-cognitive and psychosocial intervention for people with epilepsy
Testing the Efficacy of a Neuro-cognitive and Psychosocial Intervention Module in People With Epilepsy
This study is testing a new program designed to help people with drug-resistant epilepsy improve their quality of life by focusing on their thinking skills and emotional well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | All |
| Sponsor | Post Graduate Institute of Medical Education and Research, Chandigarh Academic / other |
| Locations | 1 site (Chandigarh) |
| Trial ID | NCT06537986 on ClinicalTrials.gov |
What this trial studies
This study aims to develop and test a specialized Neuro-cognitive and psychosocial intervention module for patients with drug-resistant epilepsy (DRE). It will assess the efficacy of this module in improving the quality of life for DRE patients by addressing cognitive and psychosocial issues. The study will involve a randomized control trial design, where participants will be assigned to either an intervention group receiving the module or a control group receiving standard follow-up. Comprehensive pre and post-assessments will be conducted to evaluate outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 18 to 45 with drug-resistant epilepsy who are willing to participate.
Not a fit: Patients with other neurological disorders, major psychiatric conditions, or those who cannot provide informed consent may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly enhance the quality of life for patients suffering from drug-resistant epilepsy.
How similar studies have performed: While there is limited evidence in the Indian context, similar cognitive-behavioral interventions have shown promise in other populations, indicating potential for success.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Participants of 18 - 45 years of age. 2. either gender 3. Willing to participate and sign the informed consent Exclusion Criteria: 1. Patients with other neurological disorders 2. any other trial at inclusion 3. should not have any major psychiatric disorder 4. pregnant and lactating mothers 5. also, patients who would not be giving informed consent 6. Patients with intellectual disabilities.
Where this trial is running
Chandigarh
- Post Graduate institute of medical education and research , Chandigarh — Chandigarh, India (Recruiting)
Study contacts
- Study coordinator: Neetu Choudhary, Ph.D
- Email: Neetumeel@gmail.com
- Phone: 08800136337
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.