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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.
Full description
Cognitive-Behavioral Play Therapy (CBPT) adapts Cognitive-Behavioral Therapy techniques into a play-based intervention for preschool and school-age children, especially for those facing challenges like hospitalization or chronic illnesses. Studies show that play has therapeutic value, helping children understand critical events, reduce anxiety, and cope with illness. This research aims to explore how CBPT can be applied in hospitals, specifically for children with epilepsy, to improve their quality of life, enhance problem-solving, and foster positive coping strategies. The goal is to validate CBPT as a supportive tool for enhancing psycho-emotional development and complementing medical care in hospital settings.
The study proposes a randomized controlled trial with two groups: children with epilepsy will be randomly assigned to either the cognitive-behavioral play intervention or free play. The study will assess internalizing and externalizing behaviors, coping strategies, positive thinking, problem-solving skills, and quality of life at baseline (T0) and after the 8 intervention sessions (T1).
The goal is to determine whether cognitive-behavioral play improves quality of life more than free play.
Both groups will participate in 8 weekly 40-minute play sessions, with an initial and final meeting to administer the questionnaires.
The psychologist conducting the assessments will be unaware of group assignments.
The play scenarios for both groups will be identical and based on common issues faced by children with epilepsy.
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For the purposes of the study, children aged between 6 and 10 years, of both sexes, will be recruited.
Exclusion criteria:
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52 participants in 2 patient groups
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Central trial contact
Valentina De Giorgis, MD PhD; martina p zanaboni, psy
Data sourced from clinicaltrials.gov
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