- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06583603
Identifying Barriers to Implementing Sensory Strategies in the Classroom Setting
Identifying Barriers to Implementing Sensory Strategies in the Classroom Setting: a Teacher's Perspective
The goal of this clinical trial is to determine barriers to implementing sensory strategies in the classroom setting as well as potential supports needed in teachers and paraprofessionals 18 years and older who are actively working in the classroom setting. The main questions it aims to answer are:
- What are common themes that limit classroom staff from implementing sensory strategies within the classroom setting?
- What support do classroom staff need from an occupational therapist to feel confident in implementing sensory strategies within their classroom?
Participants will be asked to participate in a 17-item electronic survey via Google Forms. They will be asked to provide informed consent prior to participating.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Allison Niemiec
- Phone Number: 413-388-8844
- Email: aflowers@baypath.edu
Study Contact Backup
- Name: Kelli Cabrera
- Email: kecabrera@baypath.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 18 years or older
- Active teacher or paraprofessional working in the classroom
Exclusion Criteria:
- Younger than 18 years old
- Teachers or paraprofessionals no longer actively working in the classroom setting
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barriers to implementing sensory strategies in the classroom setting
Time Frame: 13 weeks
|
Survey will be dispersed via email and Facebook groups.
Survey will be on google docs.
|
13 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BPU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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