Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Impact of MOHO on Therapists Working With Clients in Cancer Population (MDACC-MOHO)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01983332
Recruitment Status : Completed
First Posted : November 14, 2013
Last Update Posted : October 13, 2017
Sponsor:
Collaborator:
M.D. Anderson Cancer Center
Information provided by (Responsible Party):
Patricia Bowyer, Texas Woman's University

Brief Summary:
The purpose of this study is to examine the impact of an introduction to the occupation-based theory (MOHO) on the clinical reasoning of therapists working with cancer clients.

Condition or disease
Cancer

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.


Layout table for study information
Study Type : Observational
Actual Enrollment : 11 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Impact of the Introduction of Model of Human Occupation (MOHO) on Clinical Reasoning in Therapists Working With Clients in the Cancer Population
Actual Study Start Date : August 2013
Actual Primary Completion Date : July 2017
Actual Study Completion Date : August 2017

Group/Cohort
occupational therapists
Occupational Therapists



Primary Outcome Measures :
  1. Interviews and training sessions-observational analysis of video taped sessions [ Time Frame: 30 1/2 hours over course of year ]
    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


Secondary Outcome Measures :
  1. Observational data analysis-theme sorting until saturation reached [ Time Frame: 1 year ]
    This is a qualitative study and data will be analyzed using theme sorting until commonn themes are determined.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   25 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Participants will be outpatient-focused therapists working within the MD Anderson Cancer Center. Participants must have worked in this setting for at least 90 days before the study begins and will self-select to participate in the study. Recruitment of therapists at the MDACC will involve an introduction of the study by an onsite collaborator. The onsite collaborator will gather the names of individuals interested in participating in the study. Then, an onsite collaborator and PI will work together to determine if the therapists meet the inclusion criteria for the study. Once the therapists are determined to meet inclusion criteria, an invitation for participation will be extended by an onsite collaborator.
Criteria

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.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01983332


Locations
Layout table for location information
United States, Texas
M.D. Anderson Cancer Center
Houston, Texas, United States, 77030
Texas Woman's University
Houston, Texas, United States, 77030
Sponsors and Collaborators
Texas Woman's University
M.D. Anderson Cancer Center
Investigators
Layout table for investigator information
Principal Investigator: Patricia Bowyer, EdD,MS,OTR Texas Woman's University

Layout table for additonal information
Responsible Party: Patricia Bowyer, Patricia Bowyer, EdD, MS, OTR, FAOTA, Texas Woman's University
ClinicalTrials.gov Identifier: NCT01983332     History of Changes
Other Study ID Numbers: 17075
First Posted: November 14, 2013    Key Record Dates
Last Update Posted: October 13, 2017
Last Verified: October 2017
Keywords provided by Patricia Bowyer, Texas Woman's University:
MDACC
MOHO