functional dyspepsia or uninvestigated dyspepsia dyspepsia, functional dyspepsia, health education
Conditions
Interventions
Standard of care and receive message for health education via Line application for 4 weeks,Standard of care, do not receive message via Line application
Experimental Other,No Intervention Other
Received message via Line application,Do not receive message
Sponsors
Department of Medicine, Phramongkutklao Hospital
Eligibility
Sex/Gender
All
Age
20 Years to No maximum
Inclusion criteria
Inclusion criteria: adult aged more than 20 years old who have at least 1 of 4 following symptoms: early satiety, postprandial fullness, epigastric pain, epigastric burning for more than 1 month, never undergoing upper gastrointestinal endoscopy or undergoing upper gastrointestinal endoscopy but not found the culprit lesion, have electronic devices that be able to receive messages through the Line application.
Exclusion criteria
Exclusion criteria: patients with biliary tract disease, psychiatric disease, had the culprit lesion on endoscopy, had alarm features, pregnant, unable to take medication.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| improving of symptoms at 4 weeks after randomization Global overall Symptom scale | — |
Secondary
| Measure | Time frame |
|---|---|
| improving of symptoms at 4 weeks after randomization Short-form Leeds Dyspepsia Questionnaire,improving of symptoms at 4 weeks after randomization Likert rating 5 scales of each symptoms: indigestion, heartburn, regurgitation, nausea ,improving of symptoms at 4 weeks after randomization Adequate relieve,improving of quality of life at 4 weeks after randomization The Patient Assessment of Upper Gastrointestinal Disorders Quality of Life | — |
Countries
Thailand
Contacts
Public ContactNatee Thanupaprangsan
Phramongkutklao Hospital
Outcome results
None listed