Manual Therapy and Gastroesophageal Reflux Disease in Patients With Hiatal Hernia
Primary Purpose
Gastroesophageal Reflux
Status
Active
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Osteopathic Medicine
Control
Sponsored by
About this trial
This is an interventional treatment trial for Gastroesophageal Reflux focused on measuring Hernia, Hiatal, Osteopathic Medicine, Musculoskeletal Manipulations, Gastroesophageal Reflux
Eligibility Criteria
Inclusion Criteria:
- 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.
Exclusion Criteria:
- That fail to meet inclusion criteria.
- 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
Sites / Locations
- Ricard Tutusaus Homs
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Intervention
Control
Arm Description
Specific manual therapy for GERD and hiatal hernia
Manual therapy unrelated to GERD and hiatal hernia
Outcomes
Primary Outcome Measures
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).
Secondary Outcome Measures
Impact of GERD (Gastro-oesophageal Reflux Disease)
Using the "Gastro-oesophageal Reflux Disease impact assessment scale" used by gastroenterology team of the CSPT (Corporación Sanitaria Parc Taulí), aims to objectify GERD symptoms using a 0-10 range. The symptoms generated exclusively by the Reflux will be chosen: heartburn, regurgitation, cough, aphonia, epigastralgia. The maximum sum of the items on the scale is 50 points, indicating maximum severity. The value 0 points would indicate a minimal impact of the disease.
Quality of life in patients with GERD
For the collection of specific data on the quality of life of the patients, the QOLRAD scale will be used, this scale contains 25 items, in which the patient is asked about the effect of gastrointestinal symptoms on quality of life. Establishing the relationship with: emotional well-being, sleep, vitality, food and drink, and physical/social functioning. The patient answers the questionnaire about the frequency of these effects in relation to the last week, using a 7-point Likert scale ranging from "all the time/very much" to "never/not at all". Low scores indicate significant impairment in daily functioning (Kulich KR et al, 2005)
Full Information
NCT ID
NCT05283447
First Posted
February 18, 2022
Last Updated
March 7, 2022
Sponsor
Escoles Universitaries Gimbernat
Collaborators
Corporacion Parc Tauli
1. Study Identification
Unique Protocol Identification Number
NCT05283447
Brief Title
Manual Therapy and Gastroesophageal Reflux Disease in Patients With Hiatal Hernia
Official Title
Effectiveness of Manual Therapy in the Treatment of Gastroesophageal Reflux Disease in Patients With Type I Hiatal Hernia
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 15, 2018 (Actual)
Primary Completion Date
December 16, 2021 (Actual)
Study Completion Date
June 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Escoles Universitaries Gimbernat
Collaborators
Corporacion Parc Tauli
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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 Taulí 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastroesophageal Reflux
Keywords
Hernia, Hiatal, Osteopathic Medicine, Musculoskeletal Manipulations, Gastroesophageal Reflux
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Specific manual therapy for GERD and hiatal hernia
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Manual therapy unrelated to GERD and hiatal hernia
Intervention Type
Other
Intervention Name(s)
Osteopathic Medicine
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
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.
Primary Outcome Measure Information:
Title
Impact of GERD (Gastro-oesophageal Reflux Disease)
Description
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).
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Impact of GERD (Gastro-oesophageal Reflux Disease)
Description
Using the "Gastro-oesophageal Reflux Disease impact assessment scale" used by gastroenterology team of the CSPT (Corporación Sanitaria Parc Taulí), aims to objectify GERD symptoms using a 0-10 range. The symptoms generated exclusively by the Reflux will be chosen: heartburn, regurgitation, cough, aphonia, epigastralgia. The maximum sum of the items on the scale is 50 points, indicating maximum severity. The value 0 points would indicate a minimal impact of the disease.
Time Frame
8 weeks
Title
Quality of life in patients with GERD
Description
For the collection of specific data on the quality of life of the patients, the QOLRAD scale will be used, this scale contains 25 items, in which the patient is asked about the effect of gastrointestinal symptoms on quality of life. Establishing the relationship with: emotional well-being, sleep, vitality, food and drink, and physical/social functioning. The patient answers the questionnaire about the frequency of these effects in relation to the last week, using a 7-point Likert scale ranging from "all the time/very much" to "never/not at all". Low scores indicate significant impairment in daily functioning (Kulich KR et al, 2005)
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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.
Exclusion Criteria:
That fail to meet inclusion criteria.
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ricard Tutusaus Homs, MSc
Organizational Affiliation
EU Gimbernat
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Salvador Navarro Soto, PhD
Organizational Affiliation
Corporación Parc Taulí
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alexis Luna Aufroy, PhD
Organizational Affiliation
Corporación Parc Taulí
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Josep Maria Potau Ginés
Organizational Affiliation
Universidad de Barcelona
Official's Role
Study Director
Facility Information:
Facility Name
Ricard Tutusaus Homs
City
Sant Cugat Del Vallès
State/Province
Barcelona
ZIP/Postal Code
08174
Country
Spain
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
The pandemic has delayed the completion of the study and no publication date for the information has been proposed.
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Manual Therapy and Gastroesophageal Reflux Disease in Patients With Hiatal Hernia
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