Occupational Therapy in the Context of Head Start

Developmental Delay Clinical Trial

Official title:

An Examination of Occupational Therapy in the Context of Head Start

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01975506
• Other study ID #: 16898
• Status: Completed
• Phase: N/A
• First received: July 29, 2013
• Last updated: October 11, 2017
• Start date: November 2012
• Est. completion date: November 2016

Study information

• Verified date: October 2017
• Source: Texas Woman's University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 35
• Est. completion date: November 2016
• Est. primary completion date: November 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Developmental Delay

Locations

Country	Name	City	State
United States	Texas Woman's University	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Texas Woman's University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Model of Human Occupation(MOHO)Web Based survey	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.	The time commitment for participants will be approximately 15-20 minutes or however long it takes them to complete the online survey