The IBD-FITT Study - Moderate-intensity Exercise for IBD Patients With Moderate Disease Activity

Sponsor
University of Southern Denmark (Other)
Overall Status
Recruiting
CT.gov ID
NCT04816812
Collaborator
(none)
150
2
2
13.5
75
5.6

Study Details

Study Description

Brief Summary

The investigators aim to investigate whether exercise therapy during 12 weeks including a lesson on general healthy lifestyle in adult patients with a moderately active disease is more effective, compared to control patients only receiving a lesson on general healthy lifestyle recommendations. The three main categories of outcomes are 1) health-related quality of life, 2) general health status of the patients 3) explorative outcomes. The primary outcome is health-related quality of life, the secondary outcome is general health status measured by waist circumference, disease activity scores, blood pressure, and blood lipids, and the third outcome are explorative outcomes (none-disease specific quality of life scores, biomarkers of C-reactive protein, fecal calprotectin and immunology markers including interleukins).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise intervention
  • Behavioral: Lifestyle - online lesson intervention
N/A

Detailed Description

The investigators will apply a superior trial design in this randomized clinical trial with two arms, intervention and comparison. In both the intervention and comparison arm, the patients will receive the proper and usual medical treatment decided by their responsible physician and changes in the medical treatment is allowed at all times.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The investigators will apply a superior trial design in this randomized clinical trial with two arms, intervention, and comparison.The investigators will apply a superior trial design in this randomized clinical trial with two arms, intervention, and comparison.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The IBD-FITT Study - Moderate-intensity Exercise for Patients With Inflammatory Bowel Disease With Moderate Disease Activity: a Randomized Controlled Trial
Actual Study Start Date :
Nov 15, 2021
Anticipated Primary Completion Date :
Nov 1, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Other: Exercise

In the intervention arm, a 12-week aerobic exercise program tailored to the individual patients by physiotherapists using the principles of Frequency, Intensity, Time, and, Type (FITT) aiming to increase or maintain the physical activity level to a weekly moderate activity level.

Behavioral: Exercise intervention
A 12-week aerobic exercise program tailored to the individual patients by physiotherapists using the principles of Frequency, Intensity, Time, and, Type (FITT) aiming to increase or maintain the physical activity level to a weekly moderate activity level. This includes two supervised exercise sessions of 60 minutes per week, combined with one weekly home training session. The type of exercise is planned by a physiotherapist to fit each patient during sessions. We monitor the intervention by training diaries including frequency, intensity, time, and type of exercise (FITT) and the verbal BORG 15-point scale and heart rate monitors. We will also monitor the overall seven days' physical activity level by accelerometry using the AX3 device from the company Axivity at weeks 0 and 12.

Behavioral: Lifestyle - online lesson intervention
The investigators offer one online lesson of 15-25 minutes on lifestyle guidance including general advice on healthy living.

Other: Comparison

Comparison

Behavioral: Lifestyle - online lesson intervention
The investigators offer one online lesson of 15-25 minutes on lifestyle guidance including general advice on healthy living.

Outcome Measures

Primary Outcome Measures

  1. Inflammatory Bowel Disease Questionnaire (IBDQ) [12 weeks]

    Health-related quality of life

Secondary Outcome Measures

  1. General health - Waist circumference [12 weeks]

    Waist circumference

  2. General health - blood pressure [12 weeks]

    Blood pressure

  3. General health - Lipid [12 weeks]

    Lipid status: i. Low-density lipoprotein (LDL) ii. High-density lipoprotein (HDL) iii. Triglycerides iv. Total cholesterol v. Hemoglobin A (Hbac1)

  4. General health - Clinical disease activity [12 weeks]

    Harvey Bradshaw Index (Crohn's disease) Simple Clinical Colitis Activity Index (Ulcerative colitis)

Other Outcome Measures

  1. Explorative - European Quality of life [12 weeks]

    European Quality of life (EQ5D)

  2. Explorative - Biomarkers [12 weeks]

    i. Fecal calprotectin ii. C-reactive protein iii. Immunology (cytokines)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with moderately active Crohn's disease or ulcerative colitis are defined by fulfilling all the following five criteria:
  1. Well-characterized Crohn's disease or ulcerative colitis (physician assessment)
  1. Fulfilling standard clinical, endoscopic, radiologic, and histological criteria
  1. A minimum of one-year disease duration from the time of diagnosis of Crohn's disease or ulcerative colitis to inclusion into the trial

  2. Any of the following pharmacological treatments in a period of three months prior to inclusion:

  1. Usage of 5-Aminosalicylic acid (5-ASA) ii. Usage of corticosteroids iii. Immunomodulators usage: Azathioprine (AZA), 6-mercaptopurine (6-MP), Methotrexate (MTX) iv. Biologics usage: Anti-TNFα (Infliximab, Adalimumab, Golimumab), Ustekinumab or Anti-integrin (Vedolizumab)
  1. Disease activity defined by clinical disease score:
  1. Harvey Bradshaw Index (HBI) 27 > 5 ii. Simple Clinical Colitis Activity Index (SCCAI) 29 > 5
  1. Marker for gastrointestinal inflammation:
  1. Fecal calprotectin (FC) > 200 mg/g
Exclusion Criteria:
    1. A language barrier that prohibits the exercise instructors/supervisors to give sufficient or safe instructions during the intervention or at the general health lesson.
  1. Known heart condition that prevents them to actively participate safely in the exercise intervention.

  2. Known pregnancy or planned pregnancy. 4. Disabling musculoskeletal injuries that prevent them to actively participate in the exercise intervention.

  3. Severe disease activity manifested clinically and with the need for urgent change in treatment evaluated by the responsible physician.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital of Southwest Jutland Esbjerg Denmark
2 Odense University Hospital Odense Denmark

Sponsors and Collaborators

  • University of Southern Denmark

Investigators

  • Principal Investigator: Ken Lund, PhD, Odense University Hospital & University of Southern Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ken Lund, Principal Investigator, University of Southern Denmark
ClinicalTrials.gov Identifier:
NCT04816812
Other Study ID Numbers:
  • IBD-FITT_1
First Posted:
Mar 25, 2021
Last Update Posted:
Jan 27, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ken Lund, Principal Investigator, University of Southern Denmark
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 27, 2022