- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01975506
Occupational Therapy in the Context of Head Start
October 11, 2017 updated by: Texas Woman's University
An Examination of Occupational Therapy in the Context of Head Start
The purpose of this study is to identify the role of occupational therapy within Head Start programs.
Representatives within Head Start will be asked to participate in a nationwide internet based survey identifying the amount and type of services provided within this area.
The Model of Human Occupation (MOHO) will also be included in the study by identifying current use of the model and how it can be utilized in the future.
In order to complete this study to the fullest extent, we must begin by defining the Model of Human Occupation as well as understanding the mission of the National Head Start Association.
The vision of MOHO is to support practice that is focused on occupation, client centered, holistic, evidence-based, and complementary to other occupational therapy models.
The mission of the National Head Start Association is to coalesce, inspire and support the Head Start field as a leader in early childhood development and education.
This has lead researchers to perform the following study: An examination of occupational therapy in the context of Head Start.
Study Overview
Status
Completed
Conditions
Detailed Description
Participants will be informed of the intent of the study in the initial e-mail introduction and invitation of participation.
Participants will be given the opportunity to ask questions about the study by asking the research assistants, whose names and email addresses will be given.
Within the initial email introduction/invitation of participation, participants will be given the name and contact information of the research assistants and will be instructed to direct all questions regarding the survey to them.
All data received from the survey participants will be returned de-identified.
None of the data collected will be traceable to the survey participants.
Participants will be provided the research assistants' email addresses and can contact them should they be interested in receiving any results from the study.
The benefits of the study are to advance the overall role of Occupational Therapy services within head start facilities.
This study could further understandings of how and / or why certain concepts should / shouldn't be used, could assist administrators in developing quality programming, and contribute to the body of knowledge in Occupational Therapy in Head Start programs.
The research assistants' e-mail addresses will be provided in the consent forms with a statement saying that they will be able to contact her via e-mail should they be interested in receiving any results from the study.Informed consent will be obtained through the initial email introduction and formal request for participation.
Participants will be provided study information on the first page of the survey and will indicate their consent by clicking "yes" or "no" before beginning the survey.
Study Type
Observational
Enrollment (Actual)
35
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
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Texas
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Houston, Texas, United States, 77030
- Texas Woman's University
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Individuals within Head Start programs nationwide will be contacted to participate in an online survey about the use/role of occupational therapy in Head Start.
Particapants will be recruited to participate in the study based upon their association with Head Start organizations across the United States.
An initial e-mail will be sent to each individual informing them of the purpose of the study, and inviting them to participate in the survey.
A link to the survey along with specific instructions in how to complete it will be included in the email.
See attached email recruitment script.
The age range is from 18 and up because a variety of disciplines may be selected to respond to the survey.
Participants under the age of 18 are typically still in school and therefore may lack the exposure and understanding of occupational therapy services and the role of the occupational therapist within the Head Start program.
Description
Inclusion Criteria:
Head Start program does not discriminate against gender, so every individual over the age of 18 who works within Head Start programs will be included in this study.
Exclusion Criteria:
Although participants will not be excluded from the study based on ethnicity, non-English speaking individuals will be excluded from this study. Study materials will be presented in English only.
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
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
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head start practitioners
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Model of Human Occupation(MOHO)Web Based survey
Time Frame: The time commitment for participants will be approximately 15-20 minutes or however long it takes them to complete the online survey
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E-mail will be the primary means of completing this study.
Invitation for participation, survey instructions, and survey will all be completed through e-mail.The study will be conducted via the internet through a web based survey program.
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The time commitment for participants will be approximately 15-20 minutes or however long it takes them to complete the online survey
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Patricia Bowyer, EdD,MS,OTR, Texas Woman's 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)
November 1, 2012
Primary Completion (Actual)
November 1, 2016
Study Completion (Actual)
November 1, 2016
Study Registration Dates
First Submitted
July 29, 2013
First Submitted That Met QC Criteria
October 28, 2013
First Posted (Estimate)
November 3, 2013
Study Record Updates
Last Update Posted (Actual)
October 13, 2017
Last Update Submitted That Met QC Criteria
October 11, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 16898
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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