Music Therapy Awareness in the Lecture Hall: Effects of Mindfulness-based Breathing and Core Exercises on Stress, Endurance, and Relaxation in University Students (MT WİTH CORE)

November 25, 2025 updated by: Emine Merve Ersever, Ankara University
This study aims to evaluate the effects of music therapy awareness, mindfulness-based breathing, and core exercises on stress, resilience, and relaxation in university students. Stress is highly prevalent in this population and can negatively affect both academic performance and physical and psychological health. By combining music therapy with breathing and core exercises, the study seeks to provide a holistic approach to improving students' well-being

Study Overview

Detailed Description

University students often experience high levels of stress due to academic and social responsibilities, which may lead to reduced cognitive performance, decreased endurance, and health problems. Effective stress management strategies are therefore essential to support academic achievement and quality of life.

Music therapy has been shown to reduce stress and promote relaxation. Mindfulness-based breathing exercises enhance body awareness, calmness, and resilience, while core exercises improve physical endurance, posture, and general well-being. In a university setting, the integration of these approaches may reduce stress levels and increase both psychological and physical resilience.

This study will recruit 80 healthy volunteers aged 18-30, consisting of university students or young adults. Participants must be willing to give informed consent and must not have severe musculoskeletal, neurological, or systemic health conditions that prevent exercise. Individuals with significant hearing loss, recent surgery, or psychiatric conditions that may interfere with participation will also be excluded.

The primary objective is to investigate the effects of music therapy awareness, mindfulness-based breathing, and core exercises on stress levels, resilience, and relaxation among students. The secondary objective is to explore the potential impact of these interventions on academic performance and social relationships.

Study Type

Interventional

Enrollment (Estimated)

80

Phase

  • Not Applicable

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Healthy university students or young adults aged 18-30 years.
  • Willing to participate voluntarily and able to provide written informed consent.
  • major physical health problems or musculoskeletal injuries that would prevent participation in the exercise program, based on preliminary health screening.
  • No significant hearing impairment that would interfere with participation in music-based sessions

Exclusion Criteria:

  • Acute or chronic musculoskeletal pain, injury, or disorders that limit exercise participation.
  • Serious cardiovascular, pulmonary, or other systemic diseases that restrict physical activity.
  • History of surgery within the past 3 months or medical advice to avoid exercise
  • Psychiatric or neurological disorders that may prevent compliance with the program.
  • Significant hearing impairment or other sensory deficits that could interfere with music therapy sessions

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

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: control
Participants continue their usual activities without a structured program during the study period. Optionally, they may be offered the program after study completion
Experimental: Core exercise
Participants in the experimental group receive a combined intervention including mindfulness-based breathing exercises, core stabilization training, and music therapy sessions for stress reduction and relaxation.
Participants will engage in a structured program combining mindfulness-based breathing exercises, core stability/strength exercises, and music therapy awareness sessions. Sessions will be delivered in a lecture-hall setting, approximately 2-3 times per week, lasting 45-60 minutes, for a total duration of 4-8 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Perceived Stress Score assessed by the Perceived Stress Scale (PSS)
Time Frame: Baseline and 6 weeks

The Perceived Stress Scale (PSS) is a 10-item self-report questionnaire designed to measure the degree to which individuals perceive their lives as stressful. Each item is rated on a 5-point Likert scale ranging from 0 (never) to 4 (very often).

Total scores range from 0 to 40, with higher scores indicating greater perceived stress

Baseline and 6 weeks
Change in core muscle endurance assessed by the Plank Test
Time Frame: Baseline and 6 weeks

Core muscle endurance will be evaluated using the Plank Test. Participants are instructed to hold a standard prone plank position for as long as possible.

The time (in seconds) is recorded from the start of the position until loss of proper form or voluntary termination.

Baseline and 6 weeks
Change in core muscle endurance assessed by the Plank Test assessing by score
Time Frame: Baseline and 6 weeks
Core muscle endurance will be evaluated using the Plank Test. Scores range from 0 seconds (minimum) to the maximum duration the participant can maintain proper posture
Baseline and 6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in relaxation/calmness assessed by 5-point Likert Scale questionnaire
Time Frame: Baseline and 6 weeks
Participants rate their perceived relaxation on a 5-point Likert Scale (1 = very tense, 5 = very relaxed). Higher scores indicate greater calmness and relaxation (better outcome)
Baseline and 6 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

November 1, 2025

Primary Completion (Estimated)

February 1, 2026

Study Completion (Estimated)

April 1, 2026

Study Registration Dates

First Submitted

September 30, 2025

First Submitted That Met QC Criteria

November 25, 2025

First Posted (Actual)

November 26, 2025

Study Record Updates

Last Update Posted (Actual)

November 26, 2025

Last Update Submitted That Met QC Criteria

November 25, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • E-79176220-050.04-1961949
  • Ankara University (Other Identifier: ankara University)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL

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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