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CTRI Number  CTRI/2024/06/068257 [Registered on: 03/06/2024] Trial Registered Prospectively
Last Modified On: 30/05/2024
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Nutraceutical
Other (Specify) [Dietary intervention with aerobic exercise ]  
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Effect of FODMAP diet and aerobic exercise versus conventional therapy in patients with functional dyspepsia 
Scientific Title of Study   Epigastric symptoms response to low FODMAP diet and aerobic exercise compared with conventional therapy alone in patients with functional dyspepsia attending a tertiary care hospital in Chennai – A randomized controlled trial 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Prabhakar Davis Issac Benedict  
Designation  Department of Gastroenterology, Post graduate 2nd year  
Affiliation  Madras Medical college  
Address  Madras medical college Institute of Gastroenterology Chennai department : Department of Gastroenterology block 3
Department of gastroenterology
Chennai
TAMIL NADU
600003
India 
Phone  9629494721  
Fax    
Email  davisbenedict@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Ratnakar Kini  
Designation  Director, Department of Gastroenterology 
Affiliation  Madras Medical college  
Address  Institute of Gastroenterology Madras Medical College Chennai 600003
Department of gastroenterology Block 3 madras medical college
Chennai
TAMIL NADU
600003
India 
Phone  9629494721  
Fax    
Email  hod.mge.mmc@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Prabhakar Davis Issac Benedict  
Designation  Post graduate 2nd year  
Affiliation  Madras Medical college  
Address  Madras medical college Institute of Gastroenterology Chennai department : Department of Gastroenterology block 3

Chennai
TAMIL NADU
600003
India 
Phone  9629494721  
Fax    
Email  davisbenedict@gmail.com  
 
Source of Monetary or Material Support  
Madras medical college Institute of Gastroenterology Chennai - 600003 India department : Department of Gastroenterology block 3 infrastructure and patient support 
Self funded 
 
Primary Sponsor  
Name  Prabhakar Davis Issac Benedict  
Address  Madras MEdical COllege Institute of Gastroenterology Chennai - 600003 
Type of Sponsor  Other [self funded] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Prabhakar Davis Issac Benedict   Madras medical college and hospital  Institute of Gastroenterology Chennai department : Department of Gastroenterology block 3
Chennai
TAMIL NADU 
9629494721

davisbenedict@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional ethics committee of Madras Medical College   Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: K30||Functional dyspepsia,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Conventional therapy for functional dyspepsia and education on diet changes   - Education about diet and exercise at baseline - Assessed for SAGIS and Nepean Index at baseline, 12 and 24 weeks.  
Intervention  FODMAP diet and aerobic exercise for 12 weeks   - Education on low FODMAP diet and aerobic exercise - Diet chart and exercise chart to follow. - Alternate day mobile reminders - A calendar to mark the days the diet and exercise were followed The intervention will be given for 12 weeks. As a secondary outcome Reintroduction in the intervention group - After 12 weeks patients in the intervention group can be reintroduced to a normal diet gradually. Assessment will be done at 24 weeks with the SAGIS questionnaire to change in the SAGIS score from 12 to 24 weeks in the intervention group after the reintroduction.  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  1. Adults male and female,18-60 years with functional dyspepsia under ROME IV criteria
2. Symptoms of dyspepsia more than 6 months. (3/7 symptoms in SAGIS present)
3. Co-existing irritable bowel syndrome
4. Baseline normal Upper GI endoscopy and ECG
5. Absence of H pylori
6. Normal baseline blood investigations
7. No musculoskeletal problems
 
 
ExclusionCriteria 
Details  1. Patients not giving consent.
2. Patients already following diet plan/exercise.
3. Patients having contraindication for exercise.
4. Patients with psychiatric problems
 
 
Method of Generating Random Sequence   Random Number Table 
Method of Concealment   Not Applicable 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
Primary endpoint

Reduction in SAGIS score at 12 weeks from baseline for epigastric symptoms between intervention and control groups.
 
12 weeks 
 
Secondary Outcome  
Outcome  TimePoints 
NA  NA 
 
Target Sample Size   Total Sample Size="70"
Sample Size from India="70" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 2 
Date of First Enrollment (India)   15/06/2024 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - YES
  1. What data in particular will be shared?
    Response (Others) -  NA

  2. What additional supporting information will be shared?
    Response -  Study Protocol
    Response -  Statistical Analysis Plan
    Response - Informed Consent Form
    Response - Clinical Study Report
    Response (Others) -  NA
  3. Who will be able to view these files?
    Response (Others) -  NA

  4. For what types of analyses will this data be available?
    Response (Others) -  NA

  5. By what mechanism will data be made available?
    Response (Others) -  NA

  6. For how long will this data be available start date provided 15-11-2024 and end date provided 15-11-2028?
    Response (Others) -  NA

  7. Any URL or additional information regarding plan/policy for sharing IPD? 
    Additional Information - NIL
Brief Summary  

Introduction

The prevalence of dyspepsia in the general population is 20% (1). Among them, 80% has normal endoscopic finding. This is termed functional dyspepsia. The overall prevalence of functional dyspepsia is 22% (1). FD is divided into 1. Epigastric pain syndrome and 2. Postprandial distress syndrome. 

FODMAPs (Fructo, Oligo, Di-, Monosaccharides, And Polyols) are poorly absorbable and highly fermentable substances that cause bloating and gas sensations same as dyspepsia. 

In a study done by Heidi et al (3), on Australian patients with FD. A low FODMAP diet reduced the epigastric symptoms and overall symptoms of FD.

However, there is no evidence of the same in the Indian population.

Early data has shown promising effects of Low FODMAP in diseases other than IBS like FD

In the Indian population in a study by Goyal et al (5) with 105 patients at 4 weeks there was a reduction in FD symptoms in both groups but more in the low FODMAP group (66.7%)

The effect of aerobic exercise in patients with functional dyspepsia is still in debate. However studies have shown symptom improvement with patients on regular exercise. In a study by Siddhesh (4) et al done in Mumbai among 72 patients. Aerobic exercise for 30 mins for 5 days a week for 4 weeks GDSS (Glasgow Dyspepsia Severity Scale) before and after in the experimental population was 15.17 and 5.67 (difference = 9.5). Vs 12.83 and 8.39, respectively (difference = 4.44) in the control population. There was a significant improvement in symptoms in the patients who received exercise.

 

There is no trial studying the combined effect of Low FODMAP and aerobic exercise in patients with functional dyspepsia and its outcome.


Methodology 


Patients attending the Department of Gastroenterology who have FD under ROME IV criteria will be recruited for the study after providing detailed information on the study and consent obtained. A patient information sheet will be provided to the patient.

At baseline, patients will be assessed for symptoms of FD using the Structured Assessment of Gastrointestinal symptom (SAGIS) and the HRQOL using the Short Form Nepean Index score. The scores will be reassessed in 12 and 24 weeks of the study.

Demographic details, clinical data, and laboratory data will be collected at baseline.

Patients in the intervention group will receive.

-    Education on low FODMAP diet and aerobic exercise

-    Diet chart and exercise chart to follow.

-    Alternate day mobile reminders

-    A calendar to mark the days the diet and exercise were followed.

Reintroduction in the intervention group

-  After 12 weeks patients in the intervention group can be reintroduced to a normal diet gradually. Assessment will be done at 24 weeks with the SAGIS questionnaire to change in the SAGIS score from 12 to 24 weeks in the intervention group after the reintroduction.

Patients in the control group will receive.

-   Education about diet and exercise at baseline

    Assessed for SAGIS and Nepean Index at baseline, 12 and 24 weeks.


     Endpoints 

Primary endpoint

-    Reduction in SAGIS score at 12 weeks from baseline for epigastric symptoms between intervention and control groups.

Secondary endpoint

Overall reduction in SAGI score between intervention group and control group at 12 weeks and 24 weeks.

Reduction in the Short form Nepean Dyspepsia (SF-NDI) Index >50% from baseline between intervention and control group at 12 weeks and 24 weeks

Adherence to diet plan and exercise plan in the intervention group from the calendar

SAGI score from 12 weeks to 24 weeks after reintroduction of high FODMAP in the intervention group.


Statistical analysis

Data will be collected in pre-structured proforma and entered in an Excel sheet/EpiInfo. The data will be analyzed using SPSS version 21.

Descriptive statistics will be expressed in mean and standard deviation.

Parametric tests using the paired students’-test and non-parametric using the Mann-Whitney U test will be done. Categorical variables using the Chi-Squared test

The difference in the treatment and intervention groups will be done using the Students T-test.

 

 References 


  1. Ford AC, Mahadeva S, Carbone MF, Lacy BE, Talley NJ. Functional dyspepsia. The Lancet. 2020 Nov 21;396(10263):1689-702.
  2. Hantoro IF, Syam AF, Mudjaddid E, Setiati S, Abdullah M. Factors associated with health-related quality of life in patients with functional dyspepsia. Health and Quality of Life Outcomes. 2018 Dec;16(1):1-6.
  3. Staudacher HM, Nevin AN, Duff C, Kendall BJ, Holtmann GJ. Epigastric symptom response to low FODMAP dietary advice compared with standard dietetic advice in individuals with functional dyspepsia. Neurogastroenterology & Motility. 2021 Nov;33(11):e14148.
  4. Rane SV, Asgaonkar B, Rathi P, Contractor Q, Chandnani S, Junare P, Debnath P, Bhat V. Effect of moderate aerobic exercises on symptoms of functional dyspepsia. Indian Journal of Gastroenterology. 2021 Apr;40(2):189-97.
  5. Goyal, O., Nohria, S., Batta, S., Dhaliwal, A., Goyal, P. and Sood, A., 2022. Low fermentable oligosaccharides, disaccharides, monosaccharides, and polyols diet versus traditional dietary advice for functional dyspepsia: A randomized controlled trial. Journal of Gastroenterology and Hepatology37(2), pp.301-309.
  6. Wang B, Luo QQ, Li Q, Cheng L, Chen SL. Daily short message service reminders increase treatment compliance and efficacy in outpatients with functional dyspepsia: a prospective randomized controlled trial. Journal of general internal medicine. 2020 Oct;35(10):2925-31.

 
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