6-Minute Pegboard and Ring Test Unsupported Arm Function Exercise Test in Asthma Patients

May 2, 2020 updated by: Ebru Calik Kutukcu, Hacettepe University

Validity and Reliability of the 6-Minute Pegboard and Ring Test Unsupported Arm Function Exercise Test in Controlled and Partially Controlled Asthma Patients

Exercise intolerance is one of the most problems in chronic obstructive pulmonary disease (COPD) and occurs not only in performing lower body tasks but also in performing arm activities. During arm exercise, auxiliary respiratory muscles are used for arm duty and cannot contribute to breathing. This increases the respiratory load of the diaphragm, which is mechanically disadvantageous, and results in thoracoabdominal synchronization disorder and severe dyspnea. Although the relationship between activity limitation and quality of life is clear in patients with exertional activity, the literature on physical activity is insufficient. Exercise and physical activity can also and exercise-related respiratory symptoms are known to have adverse effects on daily living activities (ADLs). There is no gold standard for objective assessment of activity limitation and exertional dyspnea in patients with asthma. Therefore, the results obtained by evaluating the validity and reliability of the 6PRT test in asthmatic patients in this study will increase the use of this test to test both arm endurance and arm exercise capacity in adult asthmatic patients, to estimate the effect on ADLs and to demonstrate the development obtained with pulmonary rehabilitation. .

Study Overview

Status

Completed

Conditions

Detailed Description

Objective: The aim of the study was to evaluate the validity and reliability of the six-minute pegboard and ring test in patients with controlled and partially controlled asthma.

  • Demographic information: Name, age, diagnosis, occupation, body weight, height, The symptoms of the dominant and affected side, CV, family history, obstructive pulmonary diseases (dyspnoea, cough, incontinence frequency), clinical findings and respiratory function test parameters will be recorded.
  • Assessment of Respiratory Muscle Strength: With intraoral pressure measurement instrument will be measured.
  • Evaluation of Hand Grip Force: It will be measured by hand dynamometer.
  • Unarmed Arm Exercise Capacity and Arm Function / Endurance Evaluation: '6 minute Pegboard and Ring Test-6PRT'. During the test, the patient is asked to sit in front of a perforated panel and to carry as many rings as possible for six minutes to the two upper holes using two hands at the same time. Participants are attached to the test by installing a few rings before the test. Standardized encouragement is given every minute during the test. The number of rings carried for 6 minutes constitutes the final score. Before and after the test, pulse oximetry and heart rate and oxygen saturation, modified Borg scale, dyspnea, general fatigue and arm fatigue are questioned. For the validity of the test, the test will be repeated in the same patient under the same conditions every one week.

    -Evaluation of Maximal Arm Exercise Capacity: With arm ergometer limited exercise test with maximal symptoms will be evaluated and used as a criterion for the reliability of 6PRT test.

  • Daily life activities of dyspnea and breathlessness Evaluation of its Effect: The Modified Medical Research Council Scale will be evaluated with an objective measurement of 3 minutes breathing exercise test and London Chest Daily Living Activities Scale.
  • Evaluation of Postural Awareness: The validity of the Turkish version developed by Shields, Mallory & Simon in 1989 will be evaluated by the Body Awareness Survey (VFA).
  • Evaluation of Daily Living Activities: London Chest GYA Scale (25) and Milliken GYA Scale will be evaluated.
  • Assessment of Quality of Life: Disease-specific Asthma Quality of Life Scale and Health Assessment Questionnaire.
  • Asthma Control Assessment: Asthma Control Test will be evaluated.

Study Type

Observational

Enrollment (Actual)

34

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • State
      • Ankara, State, Turkey, 06100
        • Hacettepe University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Validity and reliability

Description

Inclusion Criteria:

  • To have a controlled or partially controlled asthma diagnosis, Have not experienced acute exacerbation in the last 3 months, Being between 18-80 years of age, Volunteer for research, To be able to walk and cooperate.

Exclusion Criteria:

  • To have a neurological disease or another clinical diagnosis that may affect cognitive status,
  • To have musculoskeletal and neurological disease, symptomatic heart disease, previous lung surgery and malignant disease that may affect exercise performance.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
6 minute Pegboard and Ring Test-6PRT
Time Frame: one year
Total number of rings installed within six minutes
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ebru Calik Kutukcu, Phd, Hacettepe University Physiotherapy and Rehabilitation

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 3, 2019

Primary Completion (Actual)

February 3, 2020

Study Completion (Actual)

February 3, 2020

Study Registration Dates

First Submitted

October 1, 2018

First Submitted That Met QC Criteria

October 2, 2018

First Posted (Actual)

October 3, 2018

Study Record Updates

Last Update Posted (Actual)

May 5, 2020

Last Update Submitted That Met QC Criteria

May 2, 2020

Last Verified

May 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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