NCT07646002

Brief Summary

This study aims to determine the effect of Balloon Blowing and Deep Breathing Exercise on Increasing Peripheral Oxygen Saturation in Patients with Chronic Obstructive Pulmonary Disease. The main question it aims to answer is: 1\. What is the effect of balloon blowing breathing exercise on peripheral oxygen saturation in Chronic Obstructive Pulmonary Disease patients? Participants performed the exercise on the day agreed upon with the researcher. Respondents performed balloon-blowing breathing exercises twice daily for 7 days. These exercises consisted of deep breathing exercises followed by a slow balloon-blowing technique in three cycles per session, with a 1-minute rest interval between cycles. Each cycle included a deep breath for 3-4 seconds, a breath hold for 2-3 seconds, and a slow breath into the balloon for 5-8 seconds, repeated four times. Oxygen saturation was measured after the intervention on the seventh day to assess the effect of the exercise on peripheral oxygen saturation. Researchers compared the intervention and control groups to determine whether there was a significant difference between respondents who performed deep breathing exercises and balloon-blowing (intervention) and those who performed only deep breathing exercises (control).

Trial Health

87
On Track

Trial Health Score

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

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 10, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 25, 2026

Completed
7 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

June 9, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 12, 2026

Completed
Last Updated

June 12, 2026

Status Verified

June 1, 2026

Enrollment Period

3 months

First QC Date

June 9, 2026

Last Update Submit

June 9, 2026

Conditions

Keywords

Breathing ExercisesOxygen Saturation, PeripheralBalloon Blowing ExerciseChronic Obstructive Pulmonary DiseaseDeep Breathing

Outcome Measures

Primary Outcomes (1)

  • Peripheral Oxygen Saturation

    Peripheral oxygen saturation was measured using a Braun brand pulse oximeter after the intervention on the first and seventh days to assess the effect of the exercise.

    Day 1 & Day 7

Study Arms (2)

Intervention Group

EXPERIMENTAL

Performed Balloon-blowing and Deep breathing exercises

Behavioral: Balloon-blowing and Deep breathing exercises

Control Group

EXPERIMENTAL

Performed only deep breathing exercises

Behavioral: Deep breathing exercises

Interventions

Respondents performed balloon-blowing breathing exercises twice daily for 7 days. These exercises consisted of deep breathing exercises followed by a slow balloon-blowing technique in three cycles per session, with a 1-minute rest interval between cycles. Each cycle included a deep breath for 3-4 seconds, a breath hold for 2-3 seconds, and a slow breath into the balloon for 5-8 seconds, repeated four times.

Intervention Group

The participants performed deep breathing exercises twice daily for 7 days. The exercises consisted of three cycles of deep breathing only per session, with a 1-minute rest interval between cycles. Each cycle included a deep breath in for 3-4 seconds, a breath hold for 2-3 seconds, and a slow exhalation for 5-8 seconds, repeated four times.

Control Group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Patients aged 18-60 years, diagnosed with mild to moderate COPD, or with other medical conditions but a history of COPD, able and calm to follow instructions to inhale using the balloon blowing technique, and willing to be studied with informed consent.

You may not qualify if:

  • Patients with severe shortness of breath, patients on respiratory support, and abnormal hemoglobin levels. Dropout criteria included discontinuation of the study and respondents not undergoing the appropriate intervention.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

dr. Zainoel Abidin Regional General Hospital

Banda Aceh, Special Region of Aceh, 32126, Indonesia

Location

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

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

Study Officials

  • Chairul Huda, Master & Postgraduate Program

    Indonesia University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Outcome assessors were not involved during the intervention process. Respondents were also asked not to inform the outcome assessor of the measures they received.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This study used a parallel Randomized Controlled Trial (RCT) with a 1:1 ratio
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Ns. Chairul Huda, S.Kep., M.Kep., Sp.Kep.M.B

Study Record Dates

First Submitted

June 9, 2026

First Posted

June 12, 2026

Study Start

March 10, 2026

Primary Completion

May 25, 2026

Study Completion

June 1, 2026

Last Updated

June 12, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Locations