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Determination of Forces Used in Palpatory Diagnosis

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00781144
First Posted: October 28, 2008
Last Update Posted: October 28, 2008
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.
Information provided by:
Nova Southeastern University
  Purpose
In this study, we are experimentally investigating the assessment of forces used by skilled clinicians and beginning practitioners in palpatory techniques. The study will assess pressure used during palpatory diagnosis of the paraspinal region.

Condition
Healthy Volunteers

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Effect of Experience and Gender on the Palpatory Forces Exerted by Novice and Experienced Osteopaths in Australia

Further study details as provided by Nova Southeastern University:

Primary Outcome Measures:
  • palpatory force exerted with PA springing [ Time Frame: 3 minutes ]

Enrollment: 82
Study Start Date: August 2007
Study Completion Date: August 2007
Primary Completion Date: August 2007 (Final data collection date for primary outcome measure)
Groups/Cohorts
1
first year osteopathic students
2
fourth and fifth year osteopathic students
3
experienced osteopathic clinicians

Detailed Description:
The study will assess pressure used during palpatory diagnosis of the paraspinal region. The research hypothesis is that both experience and gender will affect the amount of pressure exerted with diagnostic springing. The data will be valuable in characterizing practice parameters of novice and skilled osteopathic clinicians in palpation and will provide data on skill maturation from novice to experienced clinician. It will also allow far more precise teaching of these skills to students, who can use the transducers to determine how much pressure they are using compared to skilled clinicians. For measuring the palpatory forces, a thin film pressure transducer will be used in the hand of the clinician. Data will be collected on a portable computer via an analog to digital interface.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
first year osteopathic students, fourth and fifth year osteopathic students and experienced osteopathic clinicians
Criteria

Inclusion Criteria:

  • osteopathic student first year or senior or experienced osteopathic clinician

Exclusion Criteria:

  Contacts and Locations
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): NCT00781144


Locations
United States, Florida
Nova Southeastern University
Ft. Lauderdale, Florida, United States, 33328
Australia, Victoria
Victoria University
Melbourne, Victoria, Australia, 30001
Sponsors and Collaborators
Nova Southeastern University
Investigators
Principal Investigator: Yasmin Qureshi, MHS. MPT Nova Southeastern University, Victoria University
  More Information

Responsible Party: Yasmin Qureshi, Nova Southeastern University
ClinicalTrials.gov Identifier: NCT00781144     History of Changes
Other Study ID Numbers: HPD-OST06030201X
First Submitted: October 27, 2008
First Posted: October 28, 2008
Last Update Posted: October 28, 2008
Last Verified: October 2008