ImpACT for Developmental Coordination Disorder

NCT ID: NCT05499143

Last Updated: 2023-11-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

491 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-08-17

Study Completion Date

2022-12-17

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study investigates the impact of Developmental Coordination Disorder on the child and its environment in Belgium within the following domains: diagnosis, activities and participation, school, therapy/support, and socio-emotional impact.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Developmental Coordination Disorder

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Parents of children with DCD or related movement difficulties

Online questionnaire

Intervention Type OTHER

Online questionnaire impact for DCD - Belgian version

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Online questionnaire

Online questionnaire impact for DCD - Belgian version

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Parents of children living in Belgium
* Parents of children between 4 and 18 years old
* Parents of children who experience movement problems and/or there is a suspicion or diagnosis of DCD

Exclusion Criteria

• Parents of children who have another other medical condition that would explain the movement difficulties (e.g. cerebral palsy, muscle disease,...)
Minimum Eligible Age

4 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University Ghent

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Lynn Bar-On, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Ghent

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ghent University

Ghent, , Belgium

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Belgium

References

Explore related publications, articles, or registry entries linked to this study.

Licari MK, Alvares GA, Bernie C, Elliott C, Evans KL, McIntyre S, Pillar SV, Reynolds JE, Reid SL, Spittle AJ, Whitehouse AJO, Zwicker JG, Williams J. The unmet clinical needs of children with developmental coordination disorder. Pediatr Res. 2021 Oct;90(4):826-831. doi: 10.1038/s41390-021-01373-1. Epub 2021 Jan 27.

Reference Type BACKGROUND
PMID: 33504966 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ONZ-2022-0203

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

NDT Effectiveness Study
NCT05070910 COMPLETED NA