Viewing Study NCT03141333



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Last Modification Date: 2024-10-26 @ 12:23 PM
Study NCT ID: NCT03141333
Status: COMPLETED
Last Update Posted: 2018-05-08
First Post: 2017-04-27

Brief Title: A Teleintervention in Developmental Coordination Disorder
Sponsor: Université de Sherbrooke
Organization: Université de Sherbrooke

Study Overview

Official Title: A Randomized Feasibility Trial Evaluating a Teleintervention for Families of Children With Developmental Coordination Disorder DCD
Status: COMPLETED
Status Verified Date: 2017-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: DCD
Brief Summary: The principal study goals are to determine if a randomized control trial would be feasible particularly with regards to i recruitment and retention of parents of children having a diagnosis or a suspicion of diagnosis of DCD and ii parents utilization of the teleintervention The study will also examine quantitatively and qualitatively families acceptability of- and satisfaction with the teleintervention
Detailed Description: Developmental coordination disorder DCD is a neurodevelopmental disorder characterised by difficulties in planning and execution of motor coordination activities like dressing sports and writing Increasing parents capacity to manage their childrens needs is part of the recommended DCD best practices as soon as children are suspected to have DCD or early following diagnosis Parents capacity could be increased through simple community-based interventions using a consultative approach Using the Internet could be an interesting avenue to develop public community-based services and build parents capacity to manage their child with DCD The feasibility of recruiting and using the Internet to build parents capacity is however unknown since no such study have been conducted

This randomized feasibility trail will experiment a teleintervention characterized by a virtual interaction between a health professional and a user by Internet for children with DCD The principal study goals are to determine if a randomized control trial would be feasible particularly with regards to i recruitment and retention of parents of children having a diagnosis or a suspicion of diagnosis of DCD and ii parents utilization of the teleintervention The study will also examine quantitatively and qualitatively families acceptability of- and satisfaction with the teleintervention As part of the evaluation of acceptability the impact of the teleintervention on parental competencies will be explored At the end of the 3-months randomized feasibility trial the influence of the number of participants on the utilization of the teleintervention will be explored by providing access to the teleintervention to all participants control and intervention

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None