Physical Activity in Bronchiectasis

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Brief Title

Physical Activity in Bronchiectasis

Official Title

Patterns of Physical Activity Levels in Patients With Bronchiectasis: Cross Sectional Study Using Quantitative Methodology

Brief Summary

      The primary aim of this study is to examine the physical activity levels of patients with
      bronchiectasis.

      Subsidiary aims are:

        1. To examine whether there is a relationship between the physical activity levels of
           patients with bronchiectasis and clinical phenotype (disease severity, exercise
           capacity, quality of life or other symptoms of their disease). The investigators also
           want to explore the relationship between physical activity levels and readiness to
           change physical activity behaviour (stages of change, self-efficacy, decisional balance
           and processes of change).

        2. To assess the feasibility and acceptability of the physical activity assessment tools:
           ActiGraph, ActivPAL, pedometer and the International Physical Activity Questionnaire.

      Hypothesis:

      Patients with bronchiectasis will have low levels of physical activity, and this is related
      to their clinical phenotype (disease severity, exercise capacity, quality of life and other
      symptoms of their disease) and also their readiness to change physical activity behaviour
      (stages of change, self-efficacy, processes of change and decisional balance).
    

Detailed Description

      Bronchiectasis is the presence of abnormal, irreversibly dilated, thick walled bronchi that
      have not been caused by cystic fibrosis. Promoting physical activity and decreasing
      inactivity (e.g. sedentary periods of activity such as sitting/lying) has been proposed as a
      key component of care for chronic disease but there is no research on physical activity in
      bronchiectasis. There is research describing physical activity in other respiratory
      populations, however, the disease trajectory and demographic profile of bronchiectasis is
      sufficiently different to warrant the proposed research specifically in bronchiectasis

      The investigators need to explore physical activity in bronchiectasis and also provide
      specific information on the instruments used to measure physical activity. There are several
      methods which could be used to assess physical activity including subjective methods (e.g.
      questionnaires), objective methods (e.g. motion sensors). In this study the investigators are
      using a range of assessment tools to help determine their usefulness (feasibility and
      acceptability from the health professional and patient perspective) for quantifying physical
      activity in bronchiectasis.

      This study will also assess patients' readiness to change (stages of change, self efficacy,
      decisional balance and processes of change). Understanding patients with bronchiectasis
      readiness to change physical activity behaviour and the links between the other important
      outcome measures will help to inform a future physical activity intervention specifically in
      patients with bronchiectasis.
    


Study Type

Observational


Primary Outcome

Number of steps on the ActiGraph GT3X+ activity monitor

Secondary Outcome

 Number of steps on the ActivPAL activity monitor

Condition

Bronchiectasis


Study Arms / Comparison Groups

 Observational
Description:  Patients are asked to continue with their normal daily activities.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information



Estimated Enrollment

63

Start Date

June 2012

Completion Date

July 2013

Primary Completion Date

July 2013

Eligibility Criteria

        Inclusion Criteria:

          -  aged ≥18 years diagnosis of bronchiectasis confirmed by HRCT or CT

          -  clinically stable (no exacerbation and no significant change in symptoms or medication
             in the last four weeks)

          -  sputum bacteriology completed over the past three months

        Exclusion Criteria:

          -  clinically unstable (pulmonary exacerbation or any change in symptoms or medication in
             the last four weeks)

          -  current severe haemoptysis

          -  pregnancy or any other concomitant condition that would prevent participation
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Judy M Bradley, PhD, , 

Location Countries

United Kingdom

Location Countries

United Kingdom

Administrative Informations


NCT ID

NCT01569009

Organization ID

11/0085


Responsible Party

Principal Investigator

Study Sponsor

University of Ulster

Collaborators

 Belfast Health and Social Care Trust

Study Sponsor

Judy M Bradley, PhD, Principal Investigator, University of Ulster


Verification Date

July 2013