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Reducing Patient Memory Recall in the Burning Mouth Patient Population

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University of Pennsylvania

Status

Enrolling

Conditions

Burning Mouth Syndrome

Treatments

Other: FIRE Trial/Track Your Happiness notifications

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full description

This is a prospective study with the aims: (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.

Participants will attend 2 study visits. Visit 1 of the study will consist of screening during the baseline visit. It will include administration of questionnaires, informed consent, collection of salivary samples, helping to download the app and/or helping to set up the smartphone to receive text notifications, and assisting with the demonstration of taking surveys on smartphones.

Track Your Happiness app, a smartphone and/or text-based notification system to take surveys, will collect data on people's experiences across a random sample of the moments of their lives. Participants will receives notifications 3 times per day at random times, and will be prompted to answer questions related to the burning mouth, to exercise, and a random selection of non-clinical Track Your Happiness questions, e.g., "Are you interacting with anyone right now?" "How do you feel right now?" Participants will receive these notifications for 12 weeks.

The final study visit (visit 2) will take place 12 weeks after Visit 1. Visit 2 will consist of questionnaires and collection of salivary samples.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Individuals aged 18 years and older
  2. Willing and able to provide informed consent
  3. Have been diagnosed with BMS for at least three months by an Oral Medicine or other specialist
  4. Willing to submit a saliva sample
  5. Have continuous access to a smartphone

Exclusion criteria

  1. 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)
  2. Prior head and neck radiation and/or chemotherapy
  3. Medications that modulate or suppress the inflammatory system

Trial design

50 participants in 1 patient group

FIRE Trial Participants
Description:
This study only has one group. All participants will receive the same intervention (smart phone app/texting notifications).
Treatment:
Other: FIRE Trial/Track Your Happiness notifications

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Eugene Ko, DDS

Data sourced from clinicaltrials.gov

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