CClinicalTrials.gg
CompletedNCT01983332MDACC-MOHOUpdated Oct 13, 2017

Impact of MOHO on Therapists Working With Clients in Cancer Population

An observational study in Cancer, sponsored by Texas Woman's University. Completed at 2 sites in United States. Open to participants aged 25 Years to 65 Years. Per ClinicalTrials.gov, last updated 2017-10-13.

Sponsored by Texas Woman's University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
11
Ages
25 Years to 65 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Cancer

Keywords

  • MDACC
  • MOHO
03

In context

Lead sponsor

Texas Woman's University is the lead sponsor of 82 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 65 Years
Sexes eligible
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.

Inclusion criteria

No training in MOHO constructs,English speaking.

Exclusion criteria

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.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
11 participants (actual)
Patient registry
No

Groups and cohorts

  • occupational therapists

    Occupational Therapists

06

What researchers measure

Primary outcomes

  1. Interviews and training sessions-observational analysis of video taped sessions

    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

    Time frame: 30 1/2 hours over course of year

Secondary outcomes

  1. Observational data analysis-theme sorting until saturation reached

    This is a qualitative study and data will be analyzed using theme sorting until commonn themes are determined.

    Time frame: 1 year

07

Study locations

2 sites
  • M.D. Anderson Cancer Center
    Houston, Texas 77030, United States
  • Texas Woman's University
    Houston, Texas 77030, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 13, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01983332
Lead sponsor
Texas Woman's University
Collaborators
M.D. Anderson Cancer Center
Responsible party
Patricia Bowyer (Patricia Bowyer, EdD, MS, OTR, FAOTA, Texas Woman's University) — Principal investigator
First posted
Nov 14, 2013
Start date
Aug 2013
Primary completion
Jul 2017
Completion
Aug 2017
Last update
Oct 13, 2017

Study contacts

Patricia Bowyer, EdD,MS,OTR
principal investigator · Texas Woman's University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2017. You cannot join it, but the record below documents what was studied.

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