- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01983332
Impact of MOHO on Therapists Working With Clients in Cancer Population (MDACC-MOHO)
Impact of the Introduction of Model of Human Occupation (MOHO) on Clinical Reasoning in Therapists Working With Clients in the Cancer Population
Study Overview
Status
Conditions
Detailed Description
The study will occur at MDACC, a comprehensive cancer center in the Texas Medical Center (TMC) in Houston. The center is the largest freestanding comprehensive cancer center in the world. The facility provides inpatient and outpatient services and supports research and education.
The facility has more than 50 buildings in the greater Houston area and in central Texas. The setting for this study will be the rehabilitation services area on the main campus in the TMC.
There are private offices, conference rooms and treatment areas where video chats and monthly meetings will occur.
The study is projected to occur over a one year period. Sessions will be videotaped (video chats - initial and follow ups and monthly group meetings) for further review. Analysis of the tapes will provide data for further research and education presentations. Sessions will also be audiotaped and transcribed for further review and data analysis purposes. Neither the videotapes nor audiotapes will be shared with anyone at the facility or any uninvolved parties. Audiotapes and videotapes will be stored in locked file cabinets and password protected computers will be used to view and analyze the audio and video tapes. Only the research team will have access to the stored data locked in the file cabinet.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Texas
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Houston, Texas, United States, 77030
- M.D. Anderson Cancer Center
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Houston, Texas, United States, 77030
- Texas Woman's University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
No training in MOHO constructs,English speaking.
Exclusion Criteria:
Training in using MOHO concepts in practice, highly skilled in use of MOHO, and non-English speaking. If a therapist is skilled and knowledgeable of the constructs of MOHO, there will be no way to determine if introduction of the model has impacted a therapist's clinical reasoning. All the materials used for the study will be in English and analysis of data will be conducted by English speaking individuals, therefore the study participants must speak English.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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occupational therapists
Occupational Therapists
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Interviews and training sessions-observational analysis of video taped sessions
Time Frame: 30 1/2 hours over course of year
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The study will begin with a video chat (20-30 minutes) to attain a baseline of participants understanding of MOHO.
An initial video chat interview guide (Appendix B) will be used to facilitate the chat session and a training session on MOHO concepts (4-8 hours) will also be held (Appendix F).
The training session is a 6 part overview of the MOHO framework.
All following video chats will be conducted using the follow up video chat interview guide (Appendix C).
There will be 8 follow up video chat sessions (20-30 minutes) occurring every 6 weeks after the initial training session on MOHO concepts.
Video chat sessions will be facilitated by a research team member.
There will be 12 monthly group meetings (60-90 minutes) with all participants to allow a time to discuss use of MOHO in practice and troubleshoot issues and offer support in a formal manner.
The monthly group meeting will be facilitated by the PI and/or an onsite collaborator.
The maximum possible time commitment stands at 1830
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30 1/2 hours over course of year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Observational data analysis-theme sorting until saturation reached
Time Frame: 1 year
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This is a qualitative study and data will be analyzed using theme sorting until commonn themes are determined.
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1 year
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Patricia Bowyer, EdD,MS,OTR, Texas Woman's University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
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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