Study Stopped
Grant ended before study could be initiated
Patient Self Monitoring of Physical Therapy Exercise
Patient Self Monitoring to Transfer Physical Therapy Exercise From Clinic to Home
2 other identifiers
interventional
N/A
1 country
1
Brief Summary
Our objective is to develop an IBEHR (Image-Based Electronic Health Record) to show patients how to reproduce at home the exercises prescribed by their physical therapist (PT) in clinic. The IBEHR can also record home exercise sessions for review by and feedback from the PT. The HEALTH CARE BENEFITS of the IBEHR for patient self monitoring are: improved transfer of physical therapy exercise from clinic to home, increased adherence to the exercise prescription, and recording home exercise to assist PT decision making.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Jan 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 12, 2012
CompletedFirst Posted
Study publicly available on registry
February 1, 2013
CompletedStudy Start
First participant enrolled
January 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedDecember 10, 2014
December 1, 2014
11 months
October 12, 2012
December 8, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
adherence to physical therapy exercise
frequency (sessions, repetitions) and correctness of exercise
4 to 8 weeks
Study Arms (2)
IBEHR
ACTIVE COMPARATORIBEHR
Standard therapy
NO INTERVENTIONwritten instructions
Interventions
physical therapy device to educate patients in physical therapy exercise performance
Eligibility Criteria
You may qualify if:
- anterior knee pain or anterior cruciate ligament (ACL) injury, including non-operative and post-surgical patients
You may not qualify if:
- non computer literate
- nonambulatory
- non English speaking
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Washington
Seattle, Washington, 98195-6422, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Florence Sheehan, MD
University of Washington
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Professor
Study Record Dates
First Submitted
October 12, 2012
First Posted
February 1, 2013
Study Start
January 1, 2015
Primary Completion
December 1, 2015
Study Completion
December 1, 2015
Last Updated
December 10, 2014
Record last verified: 2014-12