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Whole Body Vibration in Chronic Obstructive Pulmonary Disease

Not Applicable
Completed
Conditions
COPD
Interventions
Device: A vertical vibration platform Fitybe
Registration Number
NCT01850173
Lead Sponsor
Hospital de Mataró
Brief Summary

The investigators designed the current study with the main objective of determining whether Whole Body Vibration Training (WBVT) alone improves muscular force and/or modifies the functional capacity parameters in severe Chronic Obstructive Pulmonary Disease (COPD) patients referred to a rehabilitation programme.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
60
Inclusion Criteria
  • severe COPD defined as a post-bronchodilator forced expiratory volume at one second (FEV1)/ forced vital capacity (FVC) < 0.7 and FEV1 < 50% predicted,
  • stable disease defined as no exacerbation,
  • hospital admission or change in treatment in the previous 3 months.
Exclusion Criteria
  • other significant respiratory disease (bronchiectasis,
  • lung fibrosis, asthma, etc),
  • active smoking,
  • severe cardiovascular,
  • neurological, and/or metabolic pathology that could interfere with the results,
  • total hip, knee or ankle arthroplasty,
  • previous vitreous haemorrhage,
  • severe alcoholism (> 80 g/day) and
  • severe malnutrition (BMI < 19 Kg/m2) to reduce the risk of falling and dropouts.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
static work with a vertical vibration platformA vertical vibration platform FitybeThe training was designed to perform static work of the lower limbs. Patients worked in a squatting position, with 30º of hip flexion and 55º of knee flexion, holding onto the bars of the WBV platform.
Primary Outcome Measures
NameTimeMethod
isokinetic knee flexor and extensor testing muscular forcebasal, 3 months follow up

the change between basal - and 3 months follow up.

distance performed in the six minutes walking test (6MWT)Basal, 3 months follow up

the change between basal - and 3 months follow up.

Secondary Outcome Measures
NameTimeMethod
respiratory muscular strength was assessed with maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP)Basal, 3 month follow up

the change between basal - and 3 months follow up.

Trial Locations

Locations (1)

Eulogio Pleguezuelos

🇪🇸

Mataró, Barcelona, Spain

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