Actively Recruiting

Phase Not Applicable
Age: 6Years - 10Years
All Genders
NCT06813612

Effect of Cognitive Behavioral Play Intervention and Epilepsy

Led by IRCCS National Neurological Institute "C. Mondino" Foundation · Updated on 2025-02-07

52

Participants Needed

1

Research Sites

103 weeks

Total Duration

On this page

Sponsors

I

IRCCS National Neurological Institute "C. Mondino" Foundation

Lead Sponsor

C

Centro Ricerca "CBPT" Roma

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess the effectiveness of Cognitive Behavioral Play Therapy interventions in patients with epilepsy. Children with epilepsy will be randomly assigned to one of two intervention conditions: the experimental group will receive cognitive-behavioral play intervention, while the control group will engage in free play. Assessments will be done at the start (T0) and end (T1) of the intervention, measuring behaviors, coping strategies, positive thinking, problem-solving, and quality of life.

CONDITIONS

Official Title

Effect of Cognitive Behavioral Play Intervention and Epilepsy

Who Can Participate

Age: 6Years - 10Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children aged 6 to 10 years
  • Children diagnosed with one of these epilepsy types: childhood self-limiting focal epilepsy, childhood absence epilepsy, self-limiting centrotemporal paroxysmal epilepsy, self-limiting epilepsy with autonomic seizures, childhood occipital epilepsy, or photosensitive occipital lobe epilepsy
Not Eligible

You will not qualify if you...

  • Children with epilepsy and cognitive disabilities as identified by IQ scores
  • Children with reduced vision or expressive hearing impairments (visually impaired or deaf)

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Child Neuropsichiatry

Pavia, Italy, 27100

Actively Recruiting

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Research Team

V

Valentina De Giorgis, MD PhD

CONTACT

M

martina p zanaboni, psy

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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