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Balance Training in Chronic Obstructive Pulmonary Disease

Balance Training: Its Effect on Pulmonary Rehabilitation of Elderly Subjects With Chronic Obstructive Pulmonary Disease

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05972239
Enrollment
21
Registered
2023-08-02
Start date
2023-05-01
Completion date
2026-01-19
Last updated
2026-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD

Keywords

Exercise, Rehabilitation, Aged, postural balance

Brief summary

The aim of the study will be to verify whether the addition of an exercise program aimed to improve balance can reduce the risk of falling in subjects with COPD over 80 years of age compared to the standard rehabilitation program. Patients will be randomly assigned in two groups (intervention and control). The pulmonary rehabilitation (PR) program is organized in accordance with current guidelines.

Detailed description

Chronic Obstructive Pulmonary Disease-COPD is the most prevalent pathology among chronic airway diseases. The average age of life has increased. Subjects over 80 years old have peculiar characteristics. Individuals with COPD have an increased risk of falling compared with healthy peers. A pulmonary rehabilitation program reduces the risk of falling as measured by gait speed. Balance training on the elderly has been shown to be effective in improving muscle strength, coordination, balance and in reducing the risk and number of falls and the fear of falling. The enrolled subjects will complete an in-patient PR program according to enrollment. Control: education, aerobic and strength training and callisthenic exercises. Intervention: education, aerobic and strength training as group Control and balance training. At baseline will be recorded: demographics and anthropometrics, comorbidities, drug therapy, flow/volume curve, arterial blood gases, serum hemoglobin, history of fall, exacerbations and risk of sarcopenia. Before and after the PR the following outcome measures will be assessed: balance performance, peripheral muscle strength, gait speed, health status, dyspnea, quality of life, exercise capacity, confidence with balance and perceived change. Sample size calculation was performed based on the primary endpoint of the study. We estimate a number of 50 subjects.

Interventions

Educational interventions, 3 individual sessions of 10-20 minutes and 1 weekly group meeting of 45-60 minutes on nutrition and on the emotional management of the disease. Supervised and incremental aerobic training, lasting at least 30 minutes, 5/6 days a week for a total of 12-14 sessions. The initial workload will be set between 50-70% of the maximum load (watts) determined starting from the 6MWT using the Hill equation and will be increased to reach a perception of moderate-intense fatigue and/or dyspnea. Supervised strength training of the lower limbs and upper limbs, lasting 30 minutes, 5/6 times a week for a total of 12-14 sessions. The workload will be calibrated to allow the execution of 12 consecutive repetitions and will be progressively increased by 0.5 kg in order to cause a moderate/intense fatigue and/or dyspnea. Group exercises aimed at improving flexibility of the trunk, lower and upper limbs, lasting at least 30 minutes, 5/6 days a week, for a total of 12-14 sessions.

OTHERBalance training added on standard pulmonary rehabilitation

Educational interventions, 3 individual sessions of 10-20 minutes and 1 weekly group meeting of 45-60 minutes on nutrition and on the emotional management of the disease. Supervised and incremental aerobic training, lasting at least 30 minutes, 5/6 days a week for a total of 12-14 sessions. The initial workload will be set between 50-70% of the maximum load determined from the 6MWT (Hill equation) and will be increased based on dyspnea. Supervised strength training of the lower limbs and upper limbs, lasting 30 minutes, 5/6 times a week for a total of 12-14 sessions. The workload will be progressively increased. Supervised balance training sessions lasting 30 minutes, 5/6 times a week for a total of 12-14 sessions. The sequence of the exercises will be personalized according to the result of the Berg Balance Scale and modified according to the progress.

Sponsors

Istituti Clinici Scientifici Maugeri SpA
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
80 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 80 years old, * Diagnosis of COPD according to GOLD Guidelines (Tiffenau Index \<70%) under optimized medical treatment, * Able to perform and complete study procedures.

Exclusion criteria

* Anticholinergic Cognitive Burden score ≥3, * Mini-Mental State Examination \<22, * Acute or chronic impairment and/or medical diseases that are likely to preclude exercise testing and PR. * Brain lesions, * Inner ear disease * Visual deficit, * Lower limb surgery in the previous 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Balance3 weeksBerg Balance Scale (BBS). Scores range from 0 (worst) - 4 (best).

Secondary

MeasureTime frameDescription
Peripheral muscle strenght3 weeksFive sit to stand test (5STS). Time \< 14.9 seconds (best), \>14.8 seconds (worst).
Gait speed3 weeks4-meter gait speed test (4MGS). Time \< 4.83 seconds (best), \>4.82 seconds (worst).
Health status3 weeksThe COPD Assessment Test (CAT) score ranges from 0 (best) to 40 (worst).
Dyspnea3 weeksMedical Research Council (mMRC) score ranges from 0 (best) to 4 (worst).
Dyspnea on daily life activities3 weeksBarthel Dyspnea Index (BDI) total score ranges from 0 (best) to 100 (worst).
COPD Quality of life3 weeksEuroQoL-5D total score ranges from 0 (worst) to 100 (best).
Exercise capacity3 weeksSix-Minute Walking Test (6MWT) measures the maximum walked distance in meters (m) in a given time (6 minutes).
Confidence with balance3 weeksActivities-specific Balance Confidence short form (ABC-6) Scale. Score from 0 (worst) to 100 (best).
Perceived change3 weeksGlobal perceived effect (GPE) scale. Score range from 1 (best) to 7 (worst).

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026