- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06619691
HOFOT Fine Motor Program
October 1, 2024 updated by: Mercy University
Hands on Fun Occupational Therapy Fine Motor Program
The aim of this study is to determine if an 8 week fine motor intervention program will lead to improve fine motor skills as measured by a standardized assessment (PDMS-3) in pre- and post-test.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The aim of this study is to determine if an 8 week fine motor intervention program will lead to improve fine motor skills as measured by a standardized assessment (Peabody Developmental Motor Scale, 3rd edition) in pre- and post-test.
The hypothesis is that a daily fine motor program will improve overall fine motor skills within 8 weeks.
Study Type
Interventional
Enrollment (Estimated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Elizabeth Berliner, MS
- Phone Number: 914-674-7688
- Email: eberliner@mercy.edu
Study Locations
-
-
New York
-
Dobbs Ferry, New York, United States, 10950
- Mercy University
-
Contact:
- Elizabeth Berliner
- Phone Number: 914-674-7688
- Email: eberliner@mercy.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- preschooler aged 3-5 years old enrolled in local preschool
Exclusion Criteria:
- None other than denial of parent consent or lack of child assent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FIne Motor Program participants
All enrolled participants will completed a fine motor intervention program over 8 weeks
|
Only intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Peabody Developmental Motor Scale, 3rd Edition
Time Frame: 8 weeks
|
Peabody Developmental Motor Scales, 3rd edition - Norm referenced and standardized assessment of fine motor skills for children ages birth-5.11
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 1, 2024
Primary Completion (Estimated)
March 1, 2025
Study Completion (Estimated)
June 1, 2025
Study Registration Dates
First Submitted
September 27, 2024
First Submitted That Met QC Criteria
September 27, 2024
First Posted (Actual)
October 1, 2024
Study Record Updates
Last Update Posted (Actual)
October 3, 2024
Last Update Submitted That Met QC Criteria
October 1, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 24-77
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.