NCT07874750

Brief Summary

The primary aim of this study is to evaluate the effects of a controlled breathing exercises-on autonomic nervous system functions (HRV) and perceived stress levels in healthy young adults with dysfunctional breathing patterns. The secondary objectives of the study are:

  • To examine changes in HRV parameters, which serve as an indicator of vagal tone.
  • To identify improvements in participants' subjective stress levels and dysfunctional breathing symptoms following the intervention. This study aims to demonstrate the efficacy of a low-cost, non-invasive, and sustainable respiratory rehabilitation strategy for clinical practice.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress45%
Sep 2026Nov 2026

Study Start

First participant enrolled

September 18, 2026

Completed
7 days until next milestone

First Submitted

Initial submission to the registry

September 25, 2026

Completed
20 days until next milestone

First Posted

Study publicly available on registry

October 15, 2026

Completed
22 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 6, 2026

Expected
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

November 20, 2026

Last Updated

October 15, 2026

Status Verified

October 1, 2026

Enrollment Period

2 months

First QC Date

September 25, 2026

Last Update Submit

October 10, 2026

Conditions

Keywords

slow-paced breathingheart rate variabilitystressdysfunctional breathing

Outcome Measures

Primary Outcomes (2)

  • heart rate variability

    Assessed using time-domain (SDNN, RMSSD) recorded by Polar H10 chest strap during rest.

    baseline and 6 weeks

  • heart rate variability

    frequency-domain (LF, HF, LF/HF ratio) parameters recorded by Polar H10 chest strap during rest.

    baseline and 6 weeks

Secondary Outcomes (2)

  • perceived stress scale

    baseline and 6 weeks

  • nijmegen questionnaire

    baseline and 6 weeks

Study Arms (2)

intervention group slow-paced breathing

EXPERIMENTAL

Participants in this group will practice a 6-week slow-paced breathing intervention

Behavioral: slow-paced breathing

control group

NO INTERVENTION

Participants in this group will not perform any breathing exercises and will continue their usual daily

Interventions

Participants in the intervention group will undergo a 6-week slow-paced breathing protocol, practicing guided slow breathing at a rate of 6 breaths per minute using a pacing application

intervention group slow-paced breathing

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy young adults aged 18 to 25 years.
  • Non-smokers.
  • Free from any chronic diseases.
  • Willingness to complete the 6-week slow-paced breathing intervention protocol.
  • Capable of understanding the study requirements and providing written informed consent.

You may not qualify if:

  • Known cardiovascular, respiratory, or severe neurological disorders.
  • History of any chronic disease.
  • Active smoking or tobacco use.
  • Current use of medications affecting heart rate or the autonomic nervous system.
  • Prior regular practice of formal slow-breathing exercises, biofeedback, or yoga breathing techniques.
  • Inability to follow the intervention protocol.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bahcesehir University, Faculty of Health Sciences, Physical Therapy and Rehabilitation laboratory

Istanbul, 34674, Turkey (Türkiye)

RECRUITING

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist and researcher

Study Record Dates

First Submitted

September 25, 2026

First Posted

October 15, 2026

Study Start

September 18, 2026

Primary Completion (Estimated)

November 6, 2026

Study Completion (Estimated)

November 20, 2026

Last Updated

October 15, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will not share

Locations