Electronic Mobile Phone App Stool Diary

Sponsor
Augusta University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04644133
Collaborator
(none)
135
1
63.8
2.1

Study Details

Study Description

Brief Summary

Our objective here is to improve the patient's compliance and accurate capture of patient reported bowel and abdominal symptoms, by utilizing a phone application that interactively records each bowel movement or leakage event and other bowel symptoms. Such an electronic stool diary may relieve the burden of using a paper daily stool diary. We will compare and validate the electronic stool diary with the paper stool diary.

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

Detailed Description

Fecal incontinence consists of multiple and often unpredictable bowel movements and leakage of stool. Chronic constipation is associated with episodes of irregular and unpredictable bowel habits and difficulty with remembering symptoms. These features lead to a recall bias, and inaccurate recollection and/or documentation of symptoms that are critical for diagnosis and management. A daily stool diary has been used in clinical trials and in clinical practice to accurately record bowel symptoms. However, patients find these diary entries cumbersome or embarrassing to use, especially with bowel movements that occur outside of home resulting in loss of data or inaccurate collection of information. Also, many patients forget events especially when this bowel habit is irregular. Therefore, it is crucial to explore new ways of accurately, reliability, and more discretely collect bowel habit information, by using current technology that a majority of people have access to.

Study Design

Study Type:
Observational
Anticipated Enrollment :
135 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Assessment of Daily Electronic Stool Diary for Constipation and Fecal Incontinence.
Actual Study Start Date :
Dec 6, 2018
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Mar 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Healthy

Subjects without bowel issues will be asked to complete a 2 week electronic stool diary and a 2 week paper stool diary. They will complete feedback questionnaires for comparison between the two forms of diaries. The subjects will have the option to download the Stool Dairy App or if they do not have access to a smartphone they will be provided with a phone on which one the app has already been uploaded and instructed on its use. Subject's charts may be reviewed.

Other: Paper diary
Subjects will be asked to complete a 2 week paper stool diary.

Other: Electronic APP diary
Subjects will be asked to complete a 2 week paper stool diary.

Constipation

Subjects diagnosed with constipation will be asked to complete a 2 week electronic stool diary and a 2 week paper stool diary. They will complete feedback questionnaires for comparison between the two forms of diaries. The subjects will have the option to download the Stool Dairy App or if they do not have access to a smartphone they will be provided with a phone on which one the app has already been uploaded and instructed on its use. Subject's charts may be reviewed.

Other: Paper diary
Subjects will be asked to complete a 2 week paper stool diary.

Other: Electronic APP diary
Subjects will be asked to complete a 2 week paper stool diary.

Fecal Incontinence

Subjects diagnosed with fecal incontinence will be asked to complete a 2 week electronic stool diary and a 2 week paper stool diary. They will complete feedback questionnaires for comparison between the two forms of diaries. The subjects will have the option to download the Stool Dairy App or if they do not have access to a smartphone they will be provided with a phone on which one the app has already been uploaded and instructed on its use. Subject's charts may be reviewed.

Other: Paper diary
Subjects will be asked to complete a 2 week paper stool diary.

Other: Electronic APP diary
Subjects will be asked to complete a 2 week paper stool diary.

Outcome Measures

Primary Outcome Measures

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

    The stool diary parameters: number of bowel movements, number of leakages, stool consistency, urgency, time spent on toilet, feeling of incomplete evacuation,straining, gas and bloating recorded in the paper form stool diary over 2 weeks will be correlated with the electronic APP stool diary parameters using Pearson correlation in healthy subjects.

  2. Correlation of electronic APP diary information with paper form stool diary in fecal incontinence subjects [2 weeks each]

    The stool diary parameters; number of bowel movements, number of leakages, stool consistency, urgency, sensation before leakage, feeling of incomplete evacuation,use of pads and medication use recorded in the paper form stool diary over 2 weeks will be correlated with the electronic APP stool diary parameters using Pearson correlation in fecal incontinence subjects

  3. The stool diary parameters [2 weeks each]

    The stool diary parameters: number of bowel movements, stool consistency, urgency, time spent on toilet, feeling of incomplete evacuation,straining, gas and bloating recorded in the paper form stool diary over 2 weeks will be correlated with the electronic APP stool diary parameters using Pearson correlation in constipation subjects

Secondary Outcome Measures

  1. Stool frequency [2 weeks]

    The number of bowel movements per week (BM), the number of spontaneous bowel movements (SBM), and the number of complete spontaneous bowel movements (CSBM) will be compared between the APP and stool diary and between healthy subjects and patients with constipation and fecal incontinence.

  2. Stool consistency [2 weeks]

    Stool consistency (Bristol Stool scale, 1-7): 1-very hard stool, 4- normal, smooth stool, 7- watery stool, will be compared between the APP and stool diary and between healthy subjects and patients with constipation and fecal incontinence.

  3. Bowel urgency [2 weeks]

    Severity of bowel urgency- unable to postpone BM for more than 15 minutes, will be compared between the APP and stool diary and between healthy subjects and patients with constipation and fecal incontinence.

  4. Stool leakage [2 weeks]

    Leakage characteristics-amount: 0- none, 1-mild, 2-moderate, 3- excessive, will be compared between the APP and stool diary and between healthy subjects and patients with fecal incontinence.

  5. Complete evacuation [2 weeks]

    Feeling of complete evacuation, will be compared between the APP and stool diary and between healthy subjects and patients with constipation and fecal incontinence.

  6. Week 1 vs Week 2 reproducibility of APP and paper diary [1 weeks]

    Compare the results for the first and the second week for the electronic APP data as well as paper data and examine the reproducibility.

  7. Straining [2 weeks]

    Stool straining will be compared between the APP and stool diary and between healthy subjects and patients with constipation.

  8. Time spent of toilet [2 weeks]

    Time spent on toilet will be compared between the APP and stool diary and between healthy subjects and patients with constipation.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Anyone older than 18 years with symptoms of Fecal Incontinence (FI), Constipation, or Healthy (i.e. no bowel issues).

  • Women of childbearing age will be asked if they are pregnant, and a confirmed negative response is given will be sufficient. No pregnancy test will be performed.

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Digestive Health Clinical Research Augusta Georgia United States 30912

Sponsors and Collaborators

  • Augusta University

Investigators

  • Study Director: Satish Rao, MD PhD, Augusta University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Satish Rao, Professor, Augusta University
ClinicalTrials.gov Identifier:
NCT04644133
Other Study ID Numbers:
  • 1297973
First Posted:
Nov 25, 2020
Last Update Posted:
Jul 21, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 21, 2022