Incorporating Patient Capacity Into the Clinical Landscape

Sponsor

Mayo Clinic (Other)

Overall Status

Completed

CT.gov ID

NCT02390570

Collaborator

(none)

111

Enrollment

Location

Arm

Actual Duration (Months)

2.8

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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	N/A

Study Design

Study Type:

Interventional

Actual Enrollment :

111 participants

Allocation:

N/A

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 :

Sep 1, 2015

Actual Primary Completion Date :

Feb 22, 2017

Actual Study Completion Date :

Dec 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
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.

Arm

Intervention/Treatment

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.

Outcome Measures

Primary Outcome Measures

Number of resource limitations measured by medical record review [Baseline up to 18 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

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.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Mayo Clinic in Rochester	Rochester	Minnesota	United States	55905

Sponsors and Collaborators

Mayo Clinic

Investigators

Principal Investigator: Kasey Boehmer, MPH, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

Responsible Party:

Kasey R. Boehmer, Health Services Analyst, Mayo Clinic

ClinicalTrials.gov Identifier:

NCT02390570

Other Study ID Numbers:

14-008621

First Posted:

Mar 17, 2015

Last Update Posted:

Jan 9, 2019

Last Verified:

Jan 1, 2019

Keywords provided by Kasey R. Boehmer, Health Services Analyst, Mayo Clinic

Patient Capacity

Additional relevant MeSH terms:

Chronic Disease

Study Results

No Results Posted as of Jan 9, 2019