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Not yet recruiting NCT07643779

Symptom Severity, Posture, Pain, and Physical Activity in Gastroesophageal Reflux Disease

Observational Gastroesophageal Reflux Disease (GERD) Symptom Musculoskeletal Pain Physical Activity

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Gastroesophageal Reflux Disease (GERD), Symptom, Musculoskeletal Pain, Physical Activity. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Investigation of Symptom Severity, Posture, Musculoskeletal Pain, and Physical Activity Levels in Patients With Gastroesophageal Reflux Disease

Overview

This study is a cross-sectional research designed to investigate symptom severity, posture, musculoskeletal pain, and physical activity levels in individuals with gastroesophageal reflux disease (GERD).

Detailed description

Symptom severity will be assessed using the GERD-Q and PROMIS GERD scales. Postural assessment will be performed using the Posture Screen Lite application. Musculoskeletal pain will be evaluated with the Visual Analog Scale (VAS) and a body diagram, while physical activity levels will be measured using the International Physical Activity Questionnaire (IPAQ).

The aim of the study is to determine whether GERD is associated not only with gastrointestinal symptoms but also with functional parameters such as posture, pain, and physical activity level.

Primary outcome measures

  • Gastroesophageal Reflux Disease Questionnaire (GERD-Q) [Time frame: 1 day]
  • PROMIS GERD Scale [Time frame: 1 day]
  • Postural Analysis [Time frame: 1 day]
  • Visual Analog Scale (VAS) [Time frame: 1 day]
  • International Physical Activity Questionnaire (IPAQ) [Time frame: 1 day]

Eligibility criteria

Inclusion criteria

  • Being diagnosed with gastroesophageal reflux disease (GERD)
  • Age between 18 and 65 years
  • Willingness to participate in the study assessments

Exclusion criteria

  • Presence of a diagnosed psychiatric disorder
  • Pregnancy or breastfeeding status

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07643779 · KBU-FTR-NC-09

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗