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Decision Making in Hypothetical Carpal Tunnel Syndrome

Primary Purpose

Carpal Tunnel Syndrome

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cost Information
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Carpal Tunnel Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • patients presenting to hand clinic OR mturk workers
  • age 18 or older

Exclusion Criteria:

  • traumatic mechanism of injury

Sites / Locations

  • Stanford Health Care

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Intervention

Arm Description

Participants in the control group will be given a hypothetical scenario about carpal tunnel syndrome and asked to make a treatment decision for that hypothetical patient.

Participants in the intervetion group will be given a hypothetical scenario about carpal tunnel syndrome as well as information about the cost of treatment and asked to make a treatment decision for that hypothetical patient.

Outcomes

Primary Outcome Measures

Decision to have Treatment
Participants are asked to answer "Should you get surgery right now," with the options of definitely yes, probably, maybe, maybe not, probably not, and definitely not

Secondary Outcome Measures

Opinion on healthcare costs
a 7 item, likert response questionnaire used to elicit participant opinions on cost in health care. This is a non-validated tool.

Full Information

First Posted
November 2, 2018
Last Updated
March 18, 2020
Sponsor
Stanford University
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1. Study Identification

Unique Protocol Identification Number
NCT03730376
Brief Title
Decision Making in Hypothetical Carpal Tunnel Syndrome
Official Title
Patient and Consumer Decision Making in a Hypothetical Case of Carpal Tunnel Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
October 1, 2018 (Actual)
Primary Completion Date
February 1, 2019 (Actual)
Study Completion Date
March 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Participants will be presented with a hypothetical scenario of carpal tunnel and asked to make a decision for that case.
Detailed Description
Participants will be randomized into 1 of 2 groups and receive a hypothetical scenario of carpal tunnel, with or without cost information, and asked to decide if that hypothetical patient should undergo a carpal tunnel release.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized into 1 of 2 study arms arm 1: control arm 2: intervention. We will use a random block generator to assign participants to their study arm.
Masking
ParticipantCare Provider
Masking Description
The care provider and patient will not be informed as to which group the participant is in
Allocation
Randomized
Enrollment
488 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants in the control group will be given a hypothetical scenario about carpal tunnel syndrome and asked to make a treatment decision for that hypothetical patient.
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Participants in the intervetion group will be given a hypothetical scenario about carpal tunnel syndrome as well as information about the cost of treatment and asked to make a treatment decision for that hypothetical patient.
Intervention Type
Other
Intervention Name(s)
Cost Information
Intervention Description
participants will be given information on the personal and societal costs
Primary Outcome Measure Information:
Title
Decision to have Treatment
Description
Participants are asked to answer "Should you get surgery right now," with the options of definitely yes, probably, maybe, maybe not, probably not, and definitely not
Time Frame
immediately after completing survey
Secondary Outcome Measure Information:
Title
Opinion on healthcare costs
Description
a 7 item, likert response questionnaire used to elicit participant opinions on cost in health care. This is a non-validated tool.
Time Frame
immediately after completing survey

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: patients presenting to hand clinic OR mturk workers age 18 or older Exclusion Criteria: traumatic mechanism of injury
Facility Information:
Facility Name
Stanford Health Care
City
Redwood City
State/Province
California
ZIP/Postal Code
94063
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Decision Making in Hypothetical Carpal Tunnel Syndrome

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