About this trial
This study is testing whether a smartphone app can help patients better follow instructions before and after shoulder surgery, compared to the usual paper instructions.
People from all backgrounds sometimes have trouble understanding or remembering everything needed to prepare for surgery and recover safely - things like when to stop certain medications, how to shower with a special soap before surgery, or how to care for a wound afterward. Missing these steps can lead to surgery being delayed or canceled, or to problems during recovery. These difficulties can be greater for patients facing barriers such as limited health information, language differences, or lack of support at home.
This study includes adults having planned shoulder arthroscopy (a type of shoulder surgery) at Johns Hopkins. Participants will be randomly assigned to one of two groups: one will receive the standard printed instructions currently used in clinic, and the other will receive the same instructions through an app on the smartphone. The app also pulls basic information from the patient's electronic health record - surgery type, date, surgeon, and medications - so instructions can be tailored to each patient. Patients using the app confirm when each step is completed, such as taking a medication or showering before surgery, and also report on how the participant is doing after surgery, which is shared with the patient's care team.
The goal is to see whether the app helps patients follow instructions more closely, improves the patient's experience and recovery, and reduces the workload on nurses and clinic staff - particularly for patients who face more barriers to care.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
scheduled for shoulder arthroscopy with participating surgeon
Disqualifiers
None
Trial design
Parallel
Treatments tested in this trial
Smartphone App-based Digital Patient Instructions
BehavioralSmartphone App-based Digital Patient Instructions
Written Patient Instructions
BehavioralWritten Patient Instructions
Treatment groups
Trial outcomes
Primary outcomes
Information Retention
Self-report of retention of patient instruction information. Participants will rate their retention of key information using a 6 item scale with a score range from 0 - 12 with higher numbers indicating greater retention.
Locations
Sponsors and contacts
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Johns Hopkins University
Lead sponsor
Frontive
Collaborator
This trial is not recruiting at the moment. You can still explore other options: