- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03645135
Does Goal Elicitation Improve Patient Perceived Involvement
April 8, 2019 updated by: Robin Kamal, Stanford University
Does Goal Elicitation Improve Patient Perceived Involvement?
The purpose of this study is to determine if goal elicitation among orthopaedic patients improves their perceived involvement in care.
Study Overview
Detailed Description
This is a RCT with 2 intervention arms.
In the first arm, the control arm, patients will be asked to complete a short questionnaire after their visit, to elicit demographic information and perceived involvement in care.
The second arm, the intervention arm, will be asked to list 2 goals for their visit and complete a short questionnaire after their visit, to elicit demographic information and perceived involvement in care.
Study Type
Interventional
Enrollment (Actual)
90
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Redwood City, California, United States, 94063
- Stanford Health Care
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- New patients visiting the orthopaedic service
- English fluency and literacy
Exclusion Criteria:
- Returning patients
- Children
- Non-English speaking patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
Patients in the control group will be asked to complete a demographics survey and assess their perceived involvement in care after their visit
|
|
|
Experimental: Goal elicitation
Patients in the intervention group will be asked to list 2 goals for their visit.
They will also be asked to complete a demographics survey and access their perceived involvement in care after their visit.
|
Patients will be asked to list 2 goals for their visit
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Involvement in Care Scale (PICS)
Time Frame: Immediately after visit
|
PICS measures the following: doctor facilitation of patient involvement, level of information exchange, and patient participation in decision making.
Scale: 0-13, higher score means higher perceived involvement.
|
Immediately after visit
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Robin N Kamal, MD, Stanford University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2018
Primary Completion (Actual)
November 19, 2018
Study Completion (Actual)
November 19, 2018
Study Registration Dates
First Submitted
August 22, 2018
First Submitted That Met QC Criteria
August 22, 2018
First Posted (Actual)
August 24, 2018
Study Record Updates
Last Update Posted (Actual)
April 10, 2019
Last Update Submitted That Met QC Criteria
April 8, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 45823
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
IPD will not be shared for this study.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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