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Health-related Physical Fitness in Patients With Inflammatory Bowel Disease

Ulcerative Colitis Clinical Trial

Official title:
The Numbers Tell the Tale: the Validation of an Assessment Battery for Health-related Physical Fitness in Patients With Inflammatory Bowel Disease

Clinical Trial Summary

Rationale: Existing literature suggests an impaired health-related physical fitness (HRPF) (i.e., body composition, aerobic capacity, muscular strength, muscular endurance, and flexibility) in patients with inflammatory bowel disease (IBD). However, previous studies did not assess HRPF with the 5- component multidimensional concept. HRPF is not routinely screened for and measured within the IBD population in clinical practice. The lack of a simple screening tool and assessment method for HRPF validated for the IBD population hinders the ability to distinguish patients with IBD with adequate physical fitness from those who might benefit from physical exercise interventions targeting specific components. Gold standard measures are too expensive and too complex to implement in daily practice and therefore a screening tool and a simpler assessment battery for HRPF validated in patients with IBD are needed. It is necessary to obtain more objective insights into the specific components of HRPF affected in patients with IBD, and its association with patient-, disease-, and treatment-related factors in order to implement systematic screening in routine care and subsequently offer tailored physical exercise interventions. Objective: The main objective of this study is to validate a simple screening tool and a best-practice assessment battery for the different components of HRPF against gold standard measures. Secondary objectives are to objectively assess the incidence of specific components affected in patients with IBD compared to healthy control subjects and to explore the association between these components of HRPF affected and patient-, disease-, and treatment-related factors.

Clinical Trial Description

The study involves one or two study visits for patients with IBD and only one study visit for healthy volunteers. During the first study visit, all participants (n=300) will perform the tests of the assessment battery for HRPF and complete several questionnaires. A representative subgroup of patients with IBD will undergo the gold standard measurements for HRPF during a second study visit. Furthermore, total physical activity measured by accelerometry will be measured in this subgroup of patients. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05482932
Study type Observational
Source Maastricht University Medical Center
Contact K. Demers, Drs.
Phone +31(0)43-3882134
Email karlijn.demers@mumc.nl
Status Not yet recruiting
Phase
Start date August 1, 2022
Completion date April 1, 2024
View Details
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