Evaluation of Impaired Mobility in Chronic Illness Constitution of a Cohort

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorUniversity Hospital, Clermont-Ferrand

About this trial

Chronic illness is a public health issue and mobility loss is frequent in this population. Among its' multiple physical and psychological consequences, increased mortality and cardiovascular morbidity seem the main concern. Therefore, the exploration of locomotor deficiencies, physical capacities and metabolism of patients with chronic illnesses constitutes a major challenge both for the treatment of causal pathologies, as well as for evaluating the impact of therapeutic interventions, the benefit of which will be an improvement in physical capacities and ultimately mobility. In view of the hypothesis of an increase in the prevalence of mobility disorders in this population, this approach is part of a logic of screening and improving the effectiveness of the care of these patients with a multidisciplinary evaluation of individual risks. The EVALMOB protocol was designed in order to try to determine a standard profile of "dysmobility" in patients with chronic illness

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Man or woman aged 18 to 90.

Patients with chronic pathology contributing to impaired mobility.

Volunteers who have given their written consent.

Affiliated to French health care system (for France)

Disqualifiers

Patients suffering from progressive psychiatric pathologies (active psychosis, hallucinations, etc.) or the presence of another serious unstabilized pathology (decompensated heart failure, progressive terminal cancer, etc.).

People with poorly controlled or unstable cardiovascular disease.

Major osteoarticular or neurological problems completely preventing the proper performance of the various tests.

Non-autonomous patient

Trial design

Design model

Single group

Treatments tested in this trial

  • Development of a screening algorithm designed to determine a "dysmobility" profile in patients with chronic illness.

    Other intervention

    Firstly, volunteers will be invited to complete online questionnaires on a secure platform. The mobility assessment will be carried out initially (t1) and up to a maximum of 4 times (t1 to t4) as part of a day hospitalization. Questionnaires will be diverse (SF36, KOOS, HOOS, BROCKER, MNA, TAMPA, etc.) in order to assess several aspects that compose mobility. Physical evaluations will include various validated tests (isokinetic strength measure, TUG, 6MWT, Berg Balance Scale, etc.)

Treatment groups

5,000 Participants
are divided into 1 treatment group
Group A: Cohort 1Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

dismobility score calculated from the results reported in secondary outcomes

The main objective being to determine patient profiles with regard to "dysmobility", all the criteria detailed as secondary outcomes will be considered for the definition of the profiles

Time frame
Day 0
2

dismobility score calculated from the results reported in secondary outcomes

The main objective being to determine patient profiles with regard to "dysmobility", all the criteria detailed as secondary outcomes will be considered for the definition of the profiles

Time frame
Month 6
3

dismobility score calculated from the results reported in secondary outcomes

The main objective being to determine patient profiles with regard to "dysmobility", all the criteria detailed as secondary outcomes will be considered for the definition of the profiles

Time frame
Year 1
4

dismobility score calculated from the results reported in secondary outcomes

The main objective being to determine patient profiles with regard to "dysmobility", all the criteria detailed as secondary outcomes will be considered for the definition of the profiles

Time frame
Year 2

Secondary outcomes

1

The main objective being to determine patient profiles with regard to "dysmobility", all the criteria detailed as secondary outcomes will be considered for the definition of the profiles

Demographics information will be obtained using a single questionnaire including questions on age, gender, qualification, personal work status, ethnicity, life and occupational events.

Time frame
Day 0
2

Weight (Kg).

Weight will be measured with the medical body weight scale SECA® and according to the ISAK recommendations.

Time frame
Day 0
3

Weight (Kg).

Weight will be measured with the medical body weight scale SECA® and according to the ISAK recommendations.

Time frame
Month 6
4

Weight (Kg).

Weight will be measured with the medical body weight scale SECA® and according to the ISAK recommendations.

Time frame
Year 1

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital, Clermont-Ferrand

Lead sponsor

I-SITE Cap 20-25 project

Collaborator