Reducing Patient Memory Recall in the Burning Mouth Patient Population

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Pennsylvania

About this trial

The goal of this study is to learn about burning mouth syndrome symptoms in real time in patients with burning mouth syndrome. The main questions it aims to answer are:

(1) To test the ability of a smartphone app to collect repeated observations of individual data to assess fluctuations in BMS symptoms (pain) at multiple points in the day as they happen; (2) To evaluate a panel of salivary biomarkers in patients with burning mouth syndrome (BMS) and to study their relationship with clinical variables. With a collaboration between Penn Dental Medicine and Wharton School of Business, our proposal aims to vastly improve the characterization of burning mouth syndrome through the use of a smartphone app and/or text-based notification.

Participants will attend 2 study visits where they will complete questionnaires and provide saliva samples and will respond to notifications/text message prompts on their smart phone 3 times a day for 12 weeks.

Eligibility criteria

Qualifiers

Individuals aged 18 years and older

Willing and able to provide informed consent

Have been diagnosed with BMS for at least three months by an Oral Medicine or other specialist

Willing to submit a saliva sample

Disqualifiers

In the opinion of the investigator, is unable or unlikely to comply fully with the study requirements or procedures for any reason (e.g. cognitive or physical impairment)

Prior head and neck radiation and/or chemotherapy

Medications that modulate or suppress the inflammatory system

Trial design

Treatments tested in this trial

  • FIRE Trial/Track Your Happiness notifications

Treatment groups

10 Participants
are divided into 1 treatment group

Sponsors and collaborators