ClinicalTrials.gg
RecruitingNCT07125521AppGERDUpdated Jun 17, 2026

Evaluating Medication Adherence of Patients With Gastroesophageal Reflux Disease With Support of the Smartphone Application GERDCare

An interventional study of GERCCare mobile app in GERD (Gastroesophageal Reflux Disease), sponsored by Institute of Gastroenterology and Hepatology, Vietnam. Recruiting at 1 site in Vietnam. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-17.

Sponsored by Institute of Gastroenterology and Hepatology, Vietnam · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Jul 2026, 3 months ago, but the record still lists the study as recruiting.
  • Started Aug 2025; still recruiting 1 year 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
380
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Adherence to GERD treatment, including medication, diet, and lifestyle, is essential for symptom control and complication prevention, yet adherence rates remain low due to various demographic and clinical factors. Digital therapeutics, particularly mobile health applications, have shown promising potential in supporting chronic disease management and improving patient outcomes.

The GERDCare mobile application was developed with direct input from gastrointestinal experts. It is designed to enhance treatment adherence and patient engagement by offering features such as educational resources, symptom tracking, medication reminders, and direct communication between patients and physicians.

The investigators are conducting a single-center, open-label, randomized controlled trial to evaluate the effectiveness of using GERDCare in improving patient adherence. Patients are followed up after four weeks of GERD treatment.

02

Conditions studied

  • GERD (Gastroesophageal Reflux Disease)

Keywords

  • GERD
  • mobile apps
  • mobile applications
  • medication adherence
03

In context

Gastroesophageal Reflux

1,211 studies on the registry are indexed under Gastroesophageal Reflux; 202 are open to participants now.

This study's planned enrollment of 380 is above the median of 68 across 796 interventional studies indexed under Gastroesophageal Reflux.

Browse Gastroesophageal Reflux studies →

Lead sponsor

Institute of Gastroenterology and Hepatology, Vietnam is the lead sponsor of 5 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • ≥18 years old
  • Presents with typical GERD symptoms (regurgitation, heartburn)
  • Owns a smartphone and capable of using smartphone applications.

Exclusion criteria

Exclusion Criteria:

  • Acute GI conditions (upper GI bleeding, acute peptic ulcer…)
  • GI (esophageal cancer, gastric cancer…)
  • Severe chronic comorbidities (heart failure, liver failure, chronic kidney disease…)
  • Pregnancy, alcohol abuse, mental health conditions impacting medication adherence or app usage
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
380 participants (estimated)

Study arms

  • Experimental
    Using GERDCare

    Using the mobile phone application GERDCare (with detailed instructions provided during recruitment)

    Other: GERCCare mobile app

  • No intervention
    Not using GERDCare

    Not using the smartphone application GERDCare

Interventions

  • OtherGERCCare mobile app

    Using the smartphone application GERDCare (with detailed instructions provided during recruitment)

06

What researchers measure

Primary outcomes

  1. Proportion of patients with good adherence at 4 weeks

    Patients achieved a score of ≥27 points on the Vietnamese Version of the General Medication Adherence Scale (GMAS). Higher scores mean better adherence.

    Time frame: 4 weeks after recruitment

Secondary outcomes

  1. Changes in GERD symptom severity

    GERD symptom severity evaluated by the Gastroesophageal Reflux Disease Questionnaire (GerdQ) Score. The score has a minimum value of 0 and a maximum value of 18. High scores present more severe GERD symptoms. Value ≥ 8 means high probability of GERD.

    Time frame: 4 weeks after recruitment

  2. Proportion of patients with clinical improvement after 4 weeks

    Symptom resolution evaluated clinically

    Time frame: 4 weeks after recruitment

  3. Changes of patients' quality of life after 4 weeks

    Patient's quality of life evaluated by the GERD Quality of Life (GERD-QoL) score. It is an 18-item questionnaire grouped into four subscales (Daily activity, Treatment effect, Diet, and Psychological well-being). The total score was converted to a scale of 0-100, in which 100 means high influence on quality of life caused by GERD symptoms.

    Time frame: 4 weeks after recruitment

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07125521
Lead sponsor
Institute of Gastroenterology and Hepatology, Vietnam
Responsible party
Sponsor
First posted
Aug 15, 2025
Start date
Aug 18, 2025
Primary completion
Jul 31, 2026 (estimated)
Completion
Aug 31, 2026 (estimated)
Last update
Jun 17, 2026

Study contacts

Binh Phuc Nguyen, MD
Contact
binhnguyen.fsh@gmail.com
+84356665787
Hang Viet Dao, MD, PhD
Contact
hangdao.fsh@gmail.com
+84987988075

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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