Trigger Finger Preference Elicitation Tool

Stanford University

Status: Terminated

Conditions: Trigger Thumb, Right Thumb; Trigger Finger, Index Finger; Trigger Finger Disorder; Trigger Thumb, Left Thumb; Trigger Finger, Little Finger; Trigger Finger, Middle Finger; Trigger Finger, Unspecified Finger; Trigger Thumb; Trigger Finger, Ring Finger; Trigger Digit; Trigger Finger; Trigger Thumb, Unspecified Thumb

Treatments: Other: handout; Other: Preference elicitation tool

Study type: Interventional

Funder types: Other

Identifiers

NCT03909490

45990

Details and patient eligibility

About

The purpose of this study is to evaluate a patient's level of decisional conflict for their treatment decision regarding their trigger finger, and study if the use of a preference elicitation tool at point of care is able to alter the level of decisional conflict

Full description

All patients presenting to the Hand Surgery clinic for evaluation of a new trigger finger will be approached for inclusion in the study. Upon diagnosis, a patient diagnosed with a trigger will be informed of the study, asked if they would like to participate, and consented into the study. Patients will then be randomized to a control group versus our test group. The control group will be given a generic handout about trigger finger and the treatment options. They will then complete the decisional conflict survey without using the tool. The second group will use the tool and then complete the decisional conflict survey.

The standard of care is not being altered- all treatment options will still be available to patients and they have select whatever option is most in line with their preference for treatment. The purpose of the tool is to facilitate preference elicitation for treatment.

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• diagnosis of trigger finger

Exclusion criteria

• prior trigger finger treatment

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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10 participants in 2 patient groups

Control

Active Comparator group

Treatment:

Other: handout

intervention- tool

Experimental group

Treatment:

Other: Preference elicitation tool