Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 11:32 PM
Ignite Modification Date:
2025-12-24 @ 11:32 PM
NCT ID:
NCT06977256
Brief Summary:
This randomized controlled trial aimed to compare the effects of a traditional sensory-based intervention and a telerehabilitation-based sensory intervention in children aged 3-7 years diagnosed with Developmental Coordination Disorder (DCD). Participants were randomly assigned to either face-to-face or combined face-to-face and telerehabilitation groups. The outcome measures included occupational performance, sensory processing, and functional independence. The study was conducted with ethical approval, and informed consent was obtained from all legal guardians.
Detailed Description:
This single-blind, parallel-group randomized controlled trial aimed to compare the effects of a traditional face-to-face sensory-based intervention and a telerehabilitation-based sensory intervention in children aged 3-7 years diagnosed with Developmental Coordination Disorder (DCD). A total of 22 participants were randomized into two groups: the Sensory-Based Intervention (SBI) group and the Telerehabilitation-Based Sensory Intervention (TBSI) group.
The SBI group received weekly 40-minute in-person sessions for 8 weeks. The TBSI group received the same 8-week in-person intervention followed by 8 weeks of weekly 30-minute telerehabilitation sessions delivered via Zoom. Both interventions included structured sensory activities tailored to each child's developmental level.
Primary and secondary outcomes were measured before and after the intervention using the Canadian Occupational Performance Measure (COPM), the Dunn Sensory Profile Parent Questionnaire, and the Functional Independence Measure for Children (WeeFIM). The study followed CONSORT guidelines and ethical approval was obtained. Written informed consent was provided by all legal guardians.
Study:
NCT06977256
Study Brief:
Protocol Section:
NCT06977256