Physiotherapy in Patients With Stable Chronic Obstructive Pulmonary Disease

Sponsor
Universidad de Granada (Other)
Overall Status
Completed
CT.gov ID
NCT02517411
Collaborator
(none)
40
1
2
9
4.4

Study Details

Study Description

Brief Summary

Chronic Obstructive Pulmonary Disease (COPD) is a lung disease that is characterized by incompletely reversible airflow obstruction. It is projected to be the fifth leading burden of disease worldwide by the year 2020. Pulmonary dysfunction reduces exercise capacity in COPD patients, and it has been previously shown that COPD patients suffer deterioration in their quality of life. The objective of this study is to examine the effects of a physical therapy intervention in stable patients with COPD.

Condition or Disease Intervention/Treatment Phase
  • Other: Standard care
  • Other: Physiotherapy added to standard care
N/A

Detailed Description

Chronic obstructive pulmonary disease (COPD) is one of the leading diseases causing mortality and morbidity, despite advanced pharmacotherapy and therapeutic management. Although COPD primarily affects the lungs, it also implies extrapulmonary manifestations, such as nutritional depletion, skeletal muscle dysfunction, and abnormal respiratory muscles.

Pulmonary rehabilitation is widely used to treat COPD patients and it has been shown that pulmonary rehabilitation should be implemented at all COPD stages, bringing them benefits in terms of improved exercise capacity, symptoms, and quality of life.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Effects of a Physiotherapy Program in Patients With Stable Chronic Obstructive Pulmonary Disease
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Jan 1, 2016
Actual Study Completion Date :
Jun 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

COPD patients with stable disease will be recruited and they will receive physiotherapy added to standard care.

Other: Physiotherapy added to standard care
The treatment will be based on domiciliary physiotherapy program during 8 weeks, twice a week added to standard care. The duration of the sessions will be 45-60 minutes. The physiotherapy treatment includes: breathing exercises, electrostimulation in quadriceps with voluntary contraction and exercises with theraband. This will be a home-based program supervised by a physiotherapist.
Other Names:
  • Physiotherapy
  • Home-based program
  • Domiciliary physiotherapy
  • Other: Control group

    COPD patients with stable disease will be recruited and they will receive standard care.

    Other: Standard care
    The standard care of stable COPD is based on long-acting bronchodilators (LABD).
    Other Names:
  • standard treatment
  • Outcome Measures

    Primary Outcome Measures

    1. Changes in Muscle strength [Baseline, 8 weeks]

      Quadriceps strength will be assessed with a portable dynamometer.

    2. Changes in Exercise capacity [Baseline, 8 weeks]

      Five times sit to stand test (5STS) will be used to assess exercise capacity, 5STS is a simple assessment tool that is feasible in all healthcare settings, and may be a rapid method of assessing changes in exercise capacity in COPD and screening for poor physical functioning individuals.

    Secondary Outcome Measures

    1. Changes in Respiratory function [Baseline, 8 weeks]

      Spirometry is regarded as the gold standard measure of respiratory function. Spirometry will be performed according to the American Thoracic Society (ATS) criteria.

    2. Changes in Dyspnea perception [Baseline, 8 weeks]

      Dyspnea perception will be assessed with Borg modified scale. Patients will classify their breathlessness between 0 and 10.

    3. Changes in Quality of life [Baseline, 8 weeks]

      EuroQol-5D (EQ-5D) will be used to assess quality of life. EQ-5D is a generic questionnaire and consists of two parts, the EQ-5D Visual analogue scale (VAS) and the EQ-5D index. The EQ-5D VAS consists on a vertical rating scale from 0 to 100 (0 = death/worst possible health state and 100 = best possible health state). The EQ-5D index is a five-item questionnaire (mobility, self-care, usual activity, pain/discomfort and anxiety/depression).

    4. Changes in Fatigue [Baseline, 8 weeks]

      Fatigue will be assessed with the Fatigue Severity Scale (FSS). The FSS is a nine-item instrument designed to assess fatigue as a symptom of a variety of different chronic conditions and disorders. The scale addresses fatigue's effects on daily functioning, querying its relationship to motivation, physical activity, work, family, and social life, and asking respondents to rate the ease with which they are fatigued and the degree to which the symptom poses a problem for them.

    5. Impact of COPD [Baseline, 8 weeks]

      The impact of COPD in patient's life will be evaluated with COPD Assessment Test (CAT) that is a simple instrument to quantify chronic obstructive pulmonary disease (COPD) impact in routine practice.

    Other Outcome Measures

    1. Quality of life related to respiratory symptoms [Baseline]

      Saint George Respiratory Questionnaire (SGRQ) will be also used to evaluate the quality of life of patients in the previous year. It includes 50 items, divided into three domains: Symptoms, Activity and Impacts. A score is calculated for each domain and a total score including all items is also obtained. Low scores indicate better health related quality of life.

    2. Peripheral vascular status [Baseline]

      Ankle-brachial index will be used to predict the presence or absence of peripheral arterial disease.

    3. Physical activity [Baseline]

      Modified Baecke Questionnaire will be used to assess the physical activity levels. It is a frequently used questionnaire to measure habitual physical activity in the elderly.

    4. Cognitive status [Baseline]

      Cognitive status will be assessed with Montreal Cognitive Assessment test (MoCA) which is a cognitive screening test designed to assist Health Professionals for detection of mild cognitive impairment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    40 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • COPD diagnosis

    • No contraindication of physiotherapy.

    • Signed written consent.

    • Medical approval for inclusion.

    Exclusion Criteria:
    • Acute exacerbation in the previous month

    • Contraindications of physiotherapy.

    • Neurological, orthopedic or heart disease.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Physical Therapy Granada Spain 18071

    Sponsors and Collaborators

    • Universidad de Granada

    Investigators

    • Principal Investigator: Marie Carmen Valenza, PhD, Universidad de Granada

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marie Carmen Valenza, PhD, Universidad de Granada
    ClinicalTrials.gov Identifier:
    NCT02517411
    Other Study ID Numbers:
    • DF0058UG
    First Posted:
    Aug 7, 2015
    Last Update Posted:
    Nov 1, 2016
    Last Verified:
    Oct 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Keywords provided by Marie Carmen Valenza, PhD, Universidad de Granada
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 1, 2016