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Pedometer Assisted Physical Activity in Individuals With COPD. A Multicenter Randomized Controlled Trial.

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
pedometer home based rehabilitation
Exercise training
Sponsored by
Yusup subagio sutanto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease (COPD) focused on measuring Pulmonary rehabilitation; Tele-medicine; Exercise capacity; Dyspnoea; Quality of life

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Individuals with COPD as defined by the Global Initiative for Chronic Obstructive Pulmonary Disease (GOLD) guidelines,2 40-80 years old, were recruited from the outpatient clinics of Moewardi and Mohammad Rabain hospitals.
  • All subjects had to be in stable conditions as assessed by absence of worsening in symptoms, i.e. no change in cough, and/or sputum beyond day-to-day variability which would have been sufficient to warrant a change in the management prescribed at discharge from hospitals or prescribed at home by their GP, and stability in blood gas values (e.g. no respiratory acidosis).

Exclusion Criteria:

  • Individuals refusing to participate, participated in a pulmonary rehabilitation program during the previous 6 months, or with active malignancy, previous lung surgery, unstable cardiovascular diseases, orthopaedic and/or neuromuscular diseases interfering with their ability to walk, or inability to connect with internet and operate WhatsApp video call applications were excluded.

Sites / Locations

  • Pulmonary department of medical faculty Universitas Sebelas Maret

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Study Group (pedometer)

Control Group

Arm Description

Participants received an Omron HJ 321 pedometer (Omron Healthcare Co Ltd, Kyoto, Japan) and were asked to walk at home at the fastest step pace as possible, for at least 30 minutes every day, up to 6 weeks.

participants received supervised exercise training at outpatient clinics for total 18 sessions (3 weekly sessions for 6 weeks).

Outcomes

Primary Outcome Measures

Exercise Tolerance
Exercise tolerance was assessed by mean of the 6MWT according to accepted

Secondary Outcome Measures

Physical Activity
Physical activity was measured as daily steps, based on an average step count of 7 days obtained from the pedometer.

Full Information

First Posted
October 17, 2021
Last Updated
October 17, 2021
Sponsor
Yusup subagio sutanto
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1. Study Identification

Unique Protocol Identification Number
NCT05098964
Brief Title
Pedometer Assisted Physical Activity in Individuals With COPD. A Multicenter Randomized Controlled Trial.
Official Title
Physical Activity in COPD
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
February 29, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Yusup subagio sutanto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Home based and tele-rehabilitation programs may be potentially useful to deliver and to maintain the benefits in difficult-to-reach areas. Tele-health technologies allow for distribution of healthcare services and exchange of information between healthcare providers and patients in different geographical locations and provide an important tool to reach people living in rural communities. In a previous single center study, we had shown that a home pedometer assisted program to enhance physical activity was as effective as and cheaper than a standard outpatient supervised exercise training program.13 We wondered whether the results of that study 13 might be confirmed in a larger multicenter randomized controlled trial (RCT). Therefore the aim of this multicenter RCT was to evaluate the benefits and costs of a program of pedometer assisted physical activity as compared to standard hospital outpatient supervised exercise training program.
Detailed Description
A multicenter RCT was conducted in Moewardi (Surakarta, Central Jawa, Indonesia) and Mohammad Rabain (Muara Enim, South Sumatra, Indonesia) hospitals from February the 1st, 2019 to February the 29th 2020. The study was performed according to the Helsinki Declaration, approved by the Committee of Moewardi Hospital, Surakarta, Central Jawa, Indonesia (Number 713/IX/HREC/2018, September 26th, 2018 and Indonesian Ministry of Health).Participants with COPD as defined by the Global Initiative for Chronic Obstructive Pulmonary Disease (GOLD) guidelines and eligible for this study were allocated into two groups using a randomly generated sequence. Before and after the program, the following outcome measures; 6MWT, BODE, physical activity, MRC and CAT Score.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease (COPD)
Keywords
Pulmonary rehabilitation; Tele-medicine; Exercise capacity; Dyspnoea; Quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Group (pedometer)
Arm Type
Experimental
Arm Description
Participants received an Omron HJ 321 pedometer (Omron Healthcare Co Ltd, Kyoto, Japan) and were asked to walk at home at the fastest step pace as possible, for at least 30 minutes every day, up to 6 weeks.
Arm Title
Control Group
Arm Type
Experimental
Arm Description
participants received supervised exercise training at outpatient clinics for total 18 sessions (3 weekly sessions for 6 weeks).
Intervention Type
Device
Intervention Name(s)
pedometer home based rehabilitation
Other Intervention Name(s)
pedometer
Intervention Description
Home based pulmonary rehabilitation for 6 weeks using pedometer Omron HJ 321 pedometer (Omron Healthcare Co Ltd, Kyoto, Japan)
Intervention Type
Other
Intervention Name(s)
Exercise training
Intervention Description
Hospital based exercise training for 6 weeks
Primary Outcome Measure Information:
Title
Exercise Tolerance
Description
Exercise tolerance was assessed by mean of the 6MWT according to accepted
Time Frame
Before and after program (6 weeks)
Secondary Outcome Measure Information:
Title
Physical Activity
Description
Physical activity was measured as daily steps, based on an average step count of 7 days obtained from the pedometer.
Time Frame
Before and after program (6 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individuals with COPD as defined by the Global Initiative for Chronic Obstructive Pulmonary Disease (GOLD) guidelines,2 40-80 years old, were recruited from the outpatient clinics of Moewardi and Mohammad Rabain hospitals. All subjects had to be in stable conditions as assessed by absence of worsening in symptoms, i.e. no change in cough, and/or sputum beyond day-to-day variability which would have been sufficient to warrant a change in the management prescribed at discharge from hospitals or prescribed at home by their GP, and stability in blood gas values (e.g. no respiratory acidosis). Exclusion Criteria: Individuals refusing to participate, participated in a pulmonary rehabilitation program during the previous 6 months, or with active malignancy, previous lung surgery, unstable cardiovascular diseases, orthopaedic and/or neuromuscular diseases interfering with their ability to walk, or inability to connect with internet and operate WhatsApp video call applications were excluded.
Facility Information:
Facility Name
Pulmonary department of medical faculty Universitas Sebelas Maret
City
Surakarta
State/Province
Central Java
ZIP/Postal Code
57126
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Pedometer Assisted Physical Activity in Individuals With COPD. A Multicenter Randomized Controlled Trial.

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