Manual Therapy and Gastroesophageal Reflux Disease in Patients With Hiatal Hernia
Effectiveness of Manual Therapy in the Treatment of Gastroesophageal Reflux Disease in Patients With Type I Hiatal Hernia
1 other identifier
interventional
44
1 country
1
Brief Summary
Introduction: Gastroesophageal reflux disease (GERD) is highly prevalent in our society. The association between GERD and hiatal hernia has been shown to be etiologically critical in the onset or worsening of these patients' clinic. Pharmacological treatment with proton pump inhibitors (IBPs) and H2 blockers is commonly prescribed and will be followed for many patients for life. The cost of health care and the effects of prolonged consumption of PPIs are questionable, and other therapeutic alternatives are being considered. Only in exceptional cases and in patients with GERD and certain types of hiatal hernia is surgery the treatment of choice. Physiotherapy at the time proposed respiratory and diaphragmatic training as a therapeutic alternative that would improve the function of anti-reflux barriers. Recently, other studies evaluating the effectiveness of manual techniques on the crural diaphragm or osteopathic maneuvers on the cervical and thoracic region have obtained good results in the improvement of the MRGE clinic. In this context, the clinical trial presented specifically treats those with reflux disease associated with a Type I hiatal hernia with manual therapy. Material and methods: The aim of the clinical study is to evaluate the effects of a clinical intervention protocol on patients with GERD for type I hiatal hernia. The variables are assessed: GERD impact using the GIS MRG Impact Scale, and the EVA format scale for the Reflux Clinic (IEPT) used by the Surgery Service of the Parc TaulĂ Hospital in Sabadell . The productivity and quality of life of these patients is also assessed using the QOLRAD reflux and dyspepsia patient quality of life questionnaire. The randomized, double-blind clinical trial has a sample of 44 patients, divided into an intervention group treated with the protocol under study, and a control group undergoing treatment that does not affect the hernia. hiatus and reflux. A total of three treatment sessions are performed on each subject. The participants answer the different questionnaires, before the start of the treatment and for each session, one week after the treatment and one month later. In the protocol, maneuvers are performed on the epigastric region, thoracic diaphragm, mediastinum and anterior face of the neck.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 18, 2022
CompletedFirst Posted
Study publicly available on registry
March 17, 2022
CompletedStudy Start
First participant enrolled
May 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 16, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2023
CompletedJuly 9, 2025
March 1, 2022
7 months
February 18, 2022
July 4, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Impact of GERD (Gastro-oesophageal Reflux Disease)
Using "The Gastro-oesophageal Reflux Disease Impact scale" (GIS).The GIS impact assessment scale consists of 9 items that refer to the frequency during the last week of 5 possible symptoms of GERD, the impact on sleep, food or drink intake, work or activities of daily living and the need to use medications in addition to those prescribed by your doctor (from "daily" to "never" on a 4-point Likert-type scale). The Gis scale score ranges from 1 to 4, the higher the score, the better the patient's condition. The scale was validated in Spanish in 2008. (New, Tafalla et al, 2008).
8 weeks
Secondary Outcomes (2)
Impact of GERD (Gastro-oesophageal Reflux Disease)
8 weeks
Quality of life in patients with GERD
8 weeks
Study Arms (2)
Intervention
EXPERIMENTALSpecific manual therapy for GERD and hiatal hernia
Control
PLACEBO COMPARATORManual therapy unrelated to GERD and hiatal hernia
Interventions
The clinical protocol subject to analysis for the intervention group consists of manual approach techniques for the myofascial and viscerofascial structures of the anterior face of the neck, maneuvers for the mediastinal region, techniques for normalizing the tone of the thoracic diaphragm and its pillars, on the peritoneal ligaments, and caudal traction of the stomach for manual correction of hiatal hernia.
The physiotherapeutic treatment on the control group consists of an approach to the lumbopelvic joint restrictions and a massage on the inframesocolic abdominal region with minimal pressure, which does not affect the activity and position of the stomach.
Eligibility Criteria
You may qualify if:
- Patients diagnosed with Gastroesophageal Reflux disease (Vakil et al, 2006)
- Age between 18 and 90 years.
- Patients with GERD due to hiatal hernia type I, without surgical indication.
- Patients with GERD due to hiatal hernia type I, with surgical indication on the waiting list.
- Patients with GERD due to hiatal hernia type I, with surgical contraindication.
You may not qualify if:
- Patients treated with Benzodiazepines (BZD)
- Patients with previous surgical interventions at the abdominal level, especially of supramesocolic structures
- Patients diagnosed with Barrett's esophagus
- Patients with paraesophageal and mixed hiatus hernias
- Diagnosed erosive esophagitis
- Active neoplasm
- Serious psychiatric disorders
- Neuromuscular or neurological injuries
- Aneurysms
- Pregnancy
- Hemophilia or treatment with anticoagulant therapy
- Hypersensitivity of the skin or dermatological diseases in the trunk that prevent the performance of the techniques
- Rejection of manual contact
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Escoles Universitaries Gimbernatlead
- Corporacion Parc Taulicollaborator
Study Sites (1)
Ricard Tutusaus Homs
Sant Cugat del Vallès, Barcelona, 08174, Spain
Related Publications (30)
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PMID: 12016131BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ricard Tutusaus Homs, MSc
EU Gimbernat
- STUDY DIRECTOR
Salvador Navarro Soto, PhD
CorporaciĂłn Parc TaulĂ
- STUDY DIRECTOR
Alexis Luna Aufroy, PhD
CorporaciĂłn Parc TaulĂ
- STUDY DIRECTOR
Josep Maria Potau Ginés
Universidad de Barcelona
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
February 18, 2022
First Posted
March 17, 2022
Study Start
May 15, 2022
Primary Completion
December 16, 2022
Study Completion
June 30, 2023
Last Updated
July 9, 2025
Record last verified: 2022-03