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Effectiveness of Telemedicine in Inflammatory Bowel Disease

Primary Purpose

Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Telemedical intervention
Sponsored by
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Inflammatory Bowel Diseases focused on measuring Inflammatory Bowel Disease, Telemedicine, Telemonitoring

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age ≥18 years old. Signed informed consent. Diagnosis: Crohn disease (ICD-10 codes K50.0, K50.1, K50.8, K50.9) and Ulcerative colitis (K51.0, K51.2, 51.3, K51.5, K51.8). Exclusion Criteria: Severe cognitive dysfunction; Acute mental illness; Lack of technical ability to take part in telemedical intervention (does not have the skills to work with a smartphone, computer, tablet, there is no appropriate technical means); Participation in other clinical studies. Oncological diseases requiring active treatment. Patients who denied signing informed consent.

Sites / Locations

  • Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Observation group

Telemedical intervention group

Arm Description

Outcomes

Primary Outcome Measures

Change the quality of life in IBD measured by SIBDQ
Change the quality of life in IBD according to Short Inflammatory Bowel Disease Questionnaire (SIBDQ). Max value is 70, min value is 10. Value less than 50 means poor heath related quality of life. Higher score means better outcome.
Change the quality of life in IBD measured by WHOQOL-26
Change the quality of life in IBD according to World Health Organization's Quality of Life (WHOQOL-26) questionnaire. Higher score means better outcome.

Secondary Outcome Measures

Maintaining/achieving clinical remission of Crohn Disease
Clinical remission of Crohn Disease will be measured by Harvey-Bradshaw Index (HBI) questionnaire. Lower score means better outcome.
Maintaining/achieving clinical remission of Ulcerative Colitis
Clinical remission of Ulcerative will be measured by Colitis Simple Clinical Colitis Activity Index (SCCAI) questionnaire. Lower score means better outcome.
Maintaining/achieving clinical remission of IBD
Clinical remission of IBD will be measured by Inflammatory Bowel Disease disk (IBD disk) questionnaire. Higher score means better outcome.
Maintaining/achieving endoscopic remission of IBD
Endoscopic remission of IBD will be measured by colonoscopy.
Maintaining/achieving histological remission of IBD
Histological remission of IBD will be measured via biopsy
Change the number adverse drug reactions in IBD
Change the number adverse drug reactions in IBD
Change satisfaction with treatment of patients with IBD
Change satisfaction with treatment of patients with IBD according to Patient Satisfaction Questionnaire (PSQ-18). Max value is 90, min value is 18. Higher score means better outcome.
Change psychological well-being of patients with IBD measured by HADS
Change psychological well-being of patients with IBD according to Hospital Anxiety and Depression Scale (HADS). Each item is scored on a response-scale with four alternatives ranging between 0 and 3. Score 8-10 for doubtful cases and ≥11 for definite cases of depression and anxiety.
Change psychological well-being of patients with IBD measured by VSI
Change psychological well-being of patients with IBD according to Visceral Sensitivity Index (VSI). Min value is 0, max value is 75. Lower score means better outcome. Score from 31 to 75 means visceral hypersensitivity.
Change psychological well-being of patients with IBD measured by TAS-26
Change psychological well-being of patients with IBD according to Toronto Alexithymia Scale (TAS-26) questionnaire. Min value 26, max value 130. Score higher than 63 means worse outcome.
Change the number of surgical interventions in IBD
Evaluation of the use of surgical interventions
Change the number of hospitalizations in IBD
Evaluation of the number of hospitalizations
Change the number of outpatient visits in IBD
Evaluation of the number of outpatient visits

Full Information

First Posted
July 21, 2023
Last Updated
August 8, 2023
Sponsor
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
Collaborators
Sechenov University
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1. Study Identification

Unique Protocol Identification Number
NCT05994716
Brief Title
Effectiveness of Telemedicine in Inflammatory Bowel Disease
Official Title
Effectiveness of Telemedicine in Inflammatory Bowel Disease
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
April 25, 2023 (Actual)
Primary Completion Date
May 30, 2024 (Anticipated)
Study Completion Date
May 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
Collaborators
Sechenov University

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
This is a prospective, randomized study to assess the impact of telemedicine (telemonitoring, tele-education and tele-consultation) on the patients with Inflammatory Bowel Disease (IBD). The main study objective is to evaluate the impact of telemedicine on the quality of life in IBD. The secondary study endpoints are to minimize adverse drug reactions, to reduce the number of IBD relapses, to improve medication adherence, to improve satisfaction with medical care, to minimize the use of healthcare resources. It is planned to enroll 60 patients. The study duration is 1 year (6 months - patient enrollment, 6 months - telemedical intervention). The study consists of 3 stages. The first stage is selection of patients with IBD after treatment in the gastroenterology department. The second stage is face-to-face appointment and general recommendations (for the observation group); monthly completion of questionnaires on the web-platform, possibility to contact with doctor via chat or phone call, access to educational information (for the intervention group). The third stage is the evaluation of IBD activity (re-hospitalization after 6 months), psychological well-being, quality of life, medication adherence, etc.
Detailed Description
Number of volunteers: 60 patients with IBD Study duration: 1 year (6 months - patient enrollment, 6 months - telemedical intervention). Inclusion criteria: Age ≥18 years old. Signed informed consent. Diagnosis: Crohn disease (ICD-10 codes K50.0, K50.1, K50.8, K50.9) and Ulcerative colitis (K51.0, K51.2, 51.3, K51.5, K51.8). Exclusion criteria: Severe cognitive dysfunction; Acute mental illness; Lack of technical ability to take part in telemedical intervention (does not have the skills to work with a smartphone, computer, tablet, there is no appropriate technical means); Participation in other clinical studies. Oncological diseases requiring active treatment. Patients who denied signing informed consent. Outpatient observation with connection to the telemonitoring program - 30 participants. Outpatient monitoring without connecting to the telemonitoring program - 30 participants. Study design: Stage 1: selection of the patients with IBD that meet the inclusion criteria after inpatient treatment in the gastroenterology department. Randomization of participants into two groups: face-to-face outpatient observation and observation using telemedicine technologies. Signing informed consent, filling out questionnaires: Simple Clinical Colitis Activity Index (SCCAI) questionnaire for patients with ulcerative colitis / Harvey-Bradshaw index (HBI) questionnaire for patients with Crohn disease; World Health Organization's Quality of Life (WHOQOL-26): questionnaire for assessing health-related quality of life; SIBDQ: Short Inflammatory Bowel Disease Questionnaire; Work Productivity and Activity Impairment Questionnaire (WPAI): questionnaire used to evaluate work productivity and activity impairment; Hospital Anxiety and Depression Scale (HADS); Toronto Alexithymia Scale (TAS-26): used to evaluate alexithymia (a risk factor for the development of psychosomatic diseases); Visceral Sensitivity Index (VSI): Special gastroenterological questionnaire to determine the index of visceral sensitivity; PSQ-18: Patient Satisfaction Questionnaire; General Medication Adherence Scale (GMAS) to determine the adherence to the therapy. Stage 2: for the outpatient observation group: one face-to-face appointment, general recommendations. For the telemonitoring group patients log in to the web platform at least once a month. When the patient log in to the telemedicine platform the following scorings must be filled out:1) SCCAI for Ulcerative colitis and Harvey-Bradshaw index for Crohn disease. 2) IBD disk questionnaire to evaluate disease dynamics. The results of the scoring systems will appear to the health care professionals and patients in a traffic light manner (red, yellow and green). If patient has a recurrence of the disease, he will be instructed to contact a doctor. Patients from intervention group will have the possibility of online consultation with a gastroenterologist upon request via chat or phone call and access to educational information about IBD, necessary lifestyle changes, dietary recommendations. To be assessed in both groups during the entire observation period: Frequency of scheduled and unscheduled visits, hospitalizations in medical organizations, assistance within the statutory health insurance system; The number of surgical interventions associated with IBD; Activity impairment and work productivity; Mortality from complications of IBD; State and patient spending on healthcare; Stage 3: re-hospitalization of both groups 6 months after randomization in order to evaluate IBD activity (laboratory and instrumental examinations). Re-completion of all questionnaires for both groups. The purpose of this study is to evaluate telemedicine impact in IBD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis
Keywords
Inflammatory Bowel Disease, Telemedicine, Telemonitoring

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Observation group
Arm Type
No Intervention
Arm Title
Telemedical intervention group
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Telemedical intervention
Intervention Description
A) Monthly completion of questionnaires on the web platform: 1) SCCAI for Ulcerative colitis and Harvey-Bradshaw index for Crohn disease. 2) IBD disk questionnaire to evaluate disease dynamics. B) Possibility of online consultation with a gastroenterologist upon request via chat or phone call. C) Access to educational information about IBD, necessary lifestyle changes, dietary recommendations.
Primary Outcome Measure Information:
Title
Change the quality of life in IBD measured by SIBDQ
Description
Change the quality of life in IBD according to Short Inflammatory Bowel Disease Questionnaire (SIBDQ). Max value is 70, min value is 10. Value less than 50 means poor heath related quality of life. Higher score means better outcome.
Time Frame
Upon completion, up to 6 months
Title
Change the quality of life in IBD measured by WHOQOL-26
Description
Change the quality of life in IBD according to World Health Organization's Quality of Life (WHOQOL-26) questionnaire. Higher score means better outcome.
Time Frame
Upon completion, up to 6 months
Secondary Outcome Measure Information:
Title
Maintaining/achieving clinical remission of Crohn Disease
Description
Clinical remission of Crohn Disease will be measured by Harvey-Bradshaw Index (HBI) questionnaire. Lower score means better outcome.
Time Frame
Upon completion, up to 6 months
Title
Maintaining/achieving clinical remission of Ulcerative Colitis
Description
Clinical remission of Ulcerative will be measured by Colitis Simple Clinical Colitis Activity Index (SCCAI) questionnaire. Lower score means better outcome.
Time Frame
Upon completion, up to 6 months
Title
Maintaining/achieving clinical remission of IBD
Description
Clinical remission of IBD will be measured by Inflammatory Bowel Disease disk (IBD disk) questionnaire. Higher score means better outcome.
Time Frame
Upon completion, up to 6 months
Title
Maintaining/achieving endoscopic remission of IBD
Description
Endoscopic remission of IBD will be measured by colonoscopy.
Time Frame
Upon completion, up to 6 months
Title
Maintaining/achieving histological remission of IBD
Description
Histological remission of IBD will be measured via biopsy
Time Frame
Upon completion, up to 6 months
Title
Change the number adverse drug reactions in IBD
Description
Change the number adverse drug reactions in IBD
Time Frame
Upon completion, up to 6 months
Title
Change satisfaction with treatment of patients with IBD
Description
Change satisfaction with treatment of patients with IBD according to Patient Satisfaction Questionnaire (PSQ-18). Max value is 90, min value is 18. Higher score means better outcome.
Time Frame
Upon completion, up to 6 months
Title
Change psychological well-being of patients with IBD measured by HADS
Description
Change psychological well-being of patients with IBD according to Hospital Anxiety and Depression Scale (HADS). Each item is scored on a response-scale with four alternatives ranging between 0 and 3. Score 8-10 for doubtful cases and ≥11 for definite cases of depression and anxiety.
Time Frame
Upon completion, up to 6 months
Title
Change psychological well-being of patients with IBD measured by VSI
Description
Change psychological well-being of patients with IBD according to Visceral Sensitivity Index (VSI). Min value is 0, max value is 75. Lower score means better outcome. Score from 31 to 75 means visceral hypersensitivity.
Time Frame
Upon completion, up to 6 months
Title
Change psychological well-being of patients with IBD measured by TAS-26
Description
Change psychological well-being of patients with IBD according to Toronto Alexithymia Scale (TAS-26) questionnaire. Min value 26, max value 130. Score higher than 63 means worse outcome.
Time Frame
Upon completion, up to 6 months
Title
Change the number of surgical interventions in IBD
Description
Evaluation of the use of surgical interventions
Time Frame
Upon completion, up to 6 months
Title
Change the number of hospitalizations in IBD
Description
Evaluation of the number of hospitalizations
Time Frame
Upon completion, up to 6 months
Title
Change the number of outpatient visits in IBD
Description
Evaluation of the number of outpatient visits
Time Frame
Upon completion, up to 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years old. Signed informed consent. Diagnosis: Crohn disease (ICD-10 codes K50.0, K50.1, K50.8, K50.9) and Ulcerative colitis (K51.0, K51.2, 51.3, K51.5, K51.8). Exclusion Criteria: Severe cognitive dysfunction; Acute mental illness; Lack of technical ability to take part in telemedical intervention (does not have the skills to work with a smartphone, computer, tablet, there is no appropriate technical means); Participation in other clinical studies. Oncological diseases requiring active treatment. Patients who denied signing informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anton V Vladzymyrskyy
Organizational Affiliation
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
Official's Role
Study Director
Facility Information:
Facility Name
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
City
Moscow
Country
Russian Federation

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effectiveness of Telemedicine in Inflammatory Bowel Disease

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