Occupational Therapy Trauma Informed Workshops and Consultations for Teachers at Head Start

August 31, 2022 updated by: Arezou Salamat, Loma Linda University

Effectiveness of Occupational Therapy Trauma Informed Workshops and Consultations for Teachers at Head Start

This study will utilize a pre/post mix method design

Quantitative data will be gathered through surveys (including satisfaction questionnaires) administered pre/post workshops.

Qualitative data will be obtained through interviews post- workshop and consultations.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

17

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 Locations

  • United States
    • California
      • Loma Linda, California, United States, 92350
        • Loma Linda University

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Home Visitors or Teaching Staff at Head Start within San Bernardino County
  • Between 18-65 years of age
  • All genders
  • English Speaking

Exclusion Criteria:

  • NA

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: Other
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Head Start Teachers
Participants will engage in three 1- hour workshops and optional consultations with an occupational therapist
Other: Workshop
Participants will engage in three 1 hour workshops about trauma informed care. They will complete pre and post measure before engaging in the workshops

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post-Survey
Time Frame: Within 1 week after the consultations

knowledge and experience

knowledge and experiences gained related to early childhood trauma. Higher scores indicate greater knowledge
Within 1 week after the consultations

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Interview
Time Frame: Within 2 weeks after the consultations
Post interviews will be completed with participants who also complete the consultations
Within 2 weeks after the consultations

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Loma Linda University

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 (Actual)

February 14, 2022

Primary Completion (Actual)

March 28, 2022

Study Completion (Actual)

April 18, 2022

Study Registration Dates

First Submitted

February 14, 2022

First Submitted That Met QC Criteria

February 28, 2022

First Posted (Actual)

March 2, 2022

Study Record Updates

Last Update Posted (Actual)

September 1, 2022

Last Update Submitted That Met QC Criteria

August 31, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 5210415

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

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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