Assessment and Validation of Electronic Gas and Bloating Diary

Sponsor
Augusta University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04684849
Collaborator
(none)
40
1
47.7
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Study Details

Study Description

Brief Summary

The investigator's goal is to improve the patient's compliance and accurate capture of patient reported gas and bloating symptoms, by utilizing a phone application that interactively records each gas and bloating event in addition to bowel events and other bowel symptoms. Such an electronic stool diary may relieve the burden of using a paper daily stool diary. The investigator will compare and validate the electronic gas and bloating diary with the paper gas and bloating diary.

Condition or Disease Intervention/Treatment Phase
  • Other: APP Diary
  • Other: Paper Diary

Detailed Description

Gas-related symptoms (GRS) such as abdominal bloating, flatulence, and belching are some of the most common gastrointestinal complaints posed by the general population. These are hallmark symptoms in patients with functional gut disorders like irritable bowel syndrome but have also been linked to conditions such as gut hypersensitivity, altered gut microbiota and altered gut motility. The main issue with grasping the full impact of these symptoms on a patients' quality of life is that they are largely subjective and thus almost impossible to standardize. However, given their pervasiveness there is merit attempting to gauge their severity in as objective a manner as possible in order to track disease progress and response to treatment. GRS can be widely irregular and requiring patients to call into the office to answer questionnaires post treatment or keep handwritten logs to turn in later can lead to inaccurate data collection that can hinder accurate diagnosis and management. The ubiquitous nature of smartphones and user-friendly interfaces of electronic applications allow for information to be logged/accessed remotely and securely, each log would have their own time stamp and be recorded in an organized, consistent manner.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Assessment and Validation of Electronic Gas and Bloating Diary
Actual Study Start Date :
Sep 10, 2020
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Aug 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Healthy subjects

Subjects who are healthy without disease

Other: APP Diary
Subjects keep a multi- item electronic digital App survey of symptoms for 2 weeks

Other: Paper Diary
Subjects keep a multi-item paper survey of symptoms for 2 weeks

Gas and Bloating patients

Patients with symptoms of gas and bloating

Other: APP Diary
Subjects keep a multi- item electronic digital App survey of symptoms for 2 weeks

Other: Paper Diary
Subjects keep a multi-item paper survey of symptoms for 2 weeks

Outcome Measures

Primary Outcome Measures

  1. Correlation of electronic APP diary information with paper form gas and bloating diary in healthy subjects [2 weeks each]

    The gas and bloating parameters recorded in the paper form gas bloating diary over 2 weeks will be correlated with the electronic APP gas and bloating diary parameters using Pearson correlation in healthy subjects

  2. Correlation of electronic APP diary information with paper form gas and bloating diary in gas and bloating subjects [2 weeks each]

    The gas and bloating parameters recorded in the paper form gas and bloating diary over 2 weeks will be correlated with the electronic APP gas and bloating diary parameters using Pearson correlation in gas and bloating subjects

Secondary Outcome Measures

  1. Flatulence (Gas) [2 weeks each]

    Frequency, duration, and severity of flatulence will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating .

  2. Abdominal distension [2 weeks each]

    Frequency, duration, and severity of abdominal distension will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating .

  3. Bloating [2 weeks each]

    Frequency, duration, and severity of bloating will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating .

  4. Abdominal Pain [2 weeks each]

    Frequency, duration, and severity of abdominal pain will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  5. Belching [2 weeks each]

    Frequency, duration, and severity of belching will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  6. Indigestion [2 weeks]

    Frequency, duration, and severity of indigestion will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  7. Nausea [2 weeks]

    Frequency, duration, and severity of nausea will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  8. Vomiting [2 weeks]

    Frequency and severity of vomiting will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  9. Number of Bowel Movements [2 weeks]

    The number of Bowel Movements will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  10. Constipation [2 weeks]

    Frequency, duration, and severity of constipation will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

  11. Diarrhea [2 weeks]

    Frequency and severity of diarrhea will be compared between the APP and gas and bloating diary and between healthy subjects and patients with gas and bloating.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion/Exclusion for gas and bloating subjects:
Inclusion:
  1. Anyone 18 to 80 years of age, inclusive with gas-related symptoms (GRS) such as gas and bloating, plus any of the following: distension, diarrhea, and/ or abdominal discomfort.

  2. Normal upper endoscopy, normal colonoscopy (<5 years) if patient is > 50 years of age, normal computerized abdominal tomography scan, or a normal right upper quadrant scan

Exclusion:
  1. Women of childbearing age will be asked if they are pregnant, and a negative response will be sufficient. No pregnancy test will be performed.

  2. History of previous GI surgeries (except for cholecystectomy, hysterectomy, and appendectomy)

  3. Significant co-morbid medical conditions, including stroke, COPD( Chronic Obstructive Pulmonary Disease) and cancers (except for non-melanotic skin cancer)

  4. Recent hospitalization within 30 days of enrollment in this study

  5. Recent History (within 4 weeks) of antibiotic use

  6. Recent History (within one week) of a colonoscopy or barium study

Inclusion/Exclusion for healthy subjects:
Inclusion:
  1. Anyone 18 to 80 years of age, inclusive with no medical problems and a negative bowel disease screening questionnaire.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Augusta University Augusta Georgia United States 30912

Sponsors and Collaborators

  • Augusta University

Investigators

  • Principal Investigator: Satish Rao, MD PhD, Augusta University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Satish Rao, Professor of Medicine, Augusta University
ClinicalTrials.gov Identifier:
NCT04684849
Other Study ID Numbers:
  • 1541299
First Posted:
Dec 28, 2020
Last Update Posted:
Jul 21, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Satish Rao, Professor of Medicine, Augusta University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 21, 2022