NCT04978831

Brief Summary

Purpose of the research; To determine the effects of wearable technology follow-up, breathing exercises with a breathing exercise device and reading aloud on vital signs, fatigue and respiratory function parameters in individuals with COPD. This research will be conducted using a randomized controlled trial model. "Personal Description Form", "COPD and Asthma Fatigue Scale", Visual Analog Scale and pulmonary function tests will be used in data collection.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
131

participants targeted

Target at P75+ for not_applicable chronic-obstructive-pulmonary-disease

Timeline
Completed

Started Nov 2020

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2020

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

July 17, 2021

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 27, 2021

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 3, 2022

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2022

Completed
Last Updated

March 31, 2022

Status Verified

March 1, 2022

Enrollment Period

1.2 years

First QC Date

July 17, 2021

Last Update Submit

March 28, 2022

Conditions

Keywords

COPDFatigueBreath exerciseReading aloud

Outcome Measures

Primary Outcomes (2)

  • Pulmonary Function Parameters

    Change in FEV1/FVC ratio will be evaluated with pulmonary function test

    2 month

  • Fatigue

    The COPD and Asthma Fatigue Scale was developed by Revicki et al in 2010 to reveal the effect of COPD and Asthma on fatigue. The items of the questions in the scale, which consists of 12 questions in total, are graded with a 5-point Likert type as "never", "rarely", "sometimes", "often", "very often". A total of 12 to 60 points is obtained from the scale. A single score is obtained from the scale for the state of fatigue, and there is no evaluation of the sub-dimensions. An increase in this score indicates that the person's fatigue level is high.

    2 month

Study Arms (3)

Respiratory exercise device group

EXPERIMENTAL
Device: PEP Device

Reading aloud group

EXPERIMENTAL
Other: Reading Aloud

Control group

NO INTERVENTION

Interventions

The breathing exercise device is a device that simulates pursed-lip breathing by creating positive expiratory pressure (PEP). Before starting to use the device, it will be explained that they need to put the mouthpiece on the device and put the nose clip on their nose, and the participants will be shown how it is done. The device will be used at 5 cmH2O pressure. A single exercise session consists of 3 exercise cycles, and a single exercise cycle consists of 15 breathing-exhalation activities. Participants will complete 3 cycles (a total of 45 inhales and exhales) in a single session. 1 loop lying on the left side, 1 loop lying on the right side, and 1 loop in sitting upright position. Participants held these sessions in the morning, afternoon, and evening. After completing each cycle, the participants will remove their nose clips and cough 2-3 times. Each participant will perform a total of 135 breathing exercises in one day.

Also known as: Smart Watch
Respiratory exercise device group

The patients in this group were given a book that they chose from among the book types within the scope of the study, according to their wishes. For the selection of books, opinions were taken from the experts in the education faculty of the same university and it was stated that any book separation was not important. The books that the participants wanted to read were provided by the researcher. They were asked to read this book aloud during the day, sitting upright on a chair or sofa, for 15 minutes, three times a day. They were able to stop reading when the participant was tired or felt too short of breath to continue reading.

Reading aloud group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Having been diagnosed with COPD for at least 6 months or before
  • Not having a respiratory system defect caused by diseases other than COPD
  • Not in the GOLD-4 COPD stage
  • Being able to read and write Turkish
  • Have no problems communicating or speaking
  • Being able to use basic information technologies
  • Using a smartphone
  • Having an active internet connection

You may not qualify if:

  • Having non-COPD pulmonary problems and diagnosed cardiovascular disease
  • Not volunteering to participate in the study
  • Having a psychiatric disorder such as schizophrenia or dementia that disrupts the thought process

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

İnönü University

Malatya, Turkey (Türkiye)

Location

Related Publications (2)

  • McNamara RJ, Epsley C, Coren E, McKeough ZJ. Singing for adults with chronic obstructive pulmonary disease (COPD). Cochrane Database Syst Rev. 2017 Dec 19;12(12):CD012296. doi: 10.1002/14651858.CD012296.pub2.

    PMID: 29253921BACKGROUND
  • Wang YT, Green JR, Nip IS, Kent RD, Kent JF. Breath group analysis for reading and spontaneous speech in healthy adults. Folia Phoniatr Logop. 2010;62(6):297-302. doi: 10.1159/000316976. Epub 2010 Jun 28.

    PMID: 20588052BACKGROUND

MeSH Terms

Conditions

Pulmonary Disease, Chronic ObstructiveDyspneaFatigue

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsRespiration DisordersSigns and Symptoms, RespiratorySigns and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

July 17, 2021

First Posted

July 27, 2021

Study Start

November 1, 2020

Primary Completion

January 3, 2022

Study Completion

January 31, 2022

Last Updated

March 31, 2022

Record last verified: 2022-03

Data Sharing

IPD Sharing
Will not share

Locations