Incorporating Patient Capacity Into the Clinical Landscape
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|ClinicalTrials.gov Identifier: NCT02390570|
Recruitment Status : Completed
First Posted : March 17, 2015
Last Update Posted : January 9, 2019
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This study is designed to answer why "patient capacity" (i.e. patient available abilities and resources to enact self-care and access healthcare) is not regularly documented in the Electronic Medical Record (EMR) in a way that is useful for clinicians.
Through the implementation of communication tools designed for patient capacity assessment and engagement of stakeholders in a process of user-centered design, the study team hypothesizes that the study can help clinicians elicit this information in conversation and regularly document it in the medical record for future healthcare discussions.
|Condition or disease||Intervention/treatment||Phase|
|Chronic Disease||Other: Patient Capacity Assessment Instrument||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||111 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Health Services Research|
|Official Title:||Incorporating Patient Capacity Into the Clinical Landscape|
|Actual Study Start Date :||September 2015|
|Actual Primary Completion Date :||February 22, 2017|
|Actual Study Completion Date :||December 2018|
|Experimental: Implementation Arm||
Other: Patient Capacity Assessment Instrument
The Patient Capacity Assessment instrument is a conversational tool designed to help patients and clinicians discuss capacity in clinicial conversations of primary care.
- Number of resource limitations measured by medical record review [ Time Frame: Baseline up to 18 months ]
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|Ages Eligible for Study:||18 Years and older (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Patients who have one or more chronic condition and do not have any barriers to consent (such as major cognitive disabilities) will be eligible for enrollment.
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): NCT02390570
|United States, Minnesota|
|Mayo Clinic in Rochester|
|Rochester, Minnesota, United States, 55905|
|Principal Investigator:||Kasey Boehmer, MPH||Mayo Clinic|
|Responsible Party:||Kasey R. Boehmer, Health Services Analyst, Mayo Clinic|
|Other Study ID Numbers:||
|First Posted:||March 17, 2015 Key Record Dates|
|Last Update Posted:||January 9, 2019|
|Last Verified:||January 2019|