The Effect of Music Accompanied Aerobic Exercise

NCT06957457 | Completed

• 1 other identifier: IstanbulMU
• Study Type: interventional
• Target: 80
• Locations: 1 country
• Sites: 1

Brief Summary

Objective: The aim of this study, which was planned as a single-blind randomized controlled design, was to investigate whether aerobic exercise accompanied by music has positive effects on pain, quality of life and well-being in patients with fibromyalgia syndrome. Materials and Methods: The study sample consisted of 80 patients diagnosed with fibromyalgia syndrome The patients were randomly assigned to either the experimental (n=40) or control group (n=40) using a computer-based randomization method. Data collection tools included the Personal Information Form , Fibromyalgia Impact Questionnaire Scale , State Anxiety Scale (STAI-I/STAI II) , Psychological Well-Being Scale

Conditions

Fibromyalgia; Fibromyalgia (FM); Syndrome Pain; Exercise

Keywords

fibromyalgia; syndrome; exercise

Outcome Measures

Primary Outcomes (1)

• Fibromyalgia Impact Questionnaire Scale

  The first item in the questionnaire includes a scale of 0-3 (0: always 1: most of the time 2: sometimes 3: never) for 11 activities of daily living such as shopping, laundry, cooking, making beds, washing dishes by hand, vacuuming carpets, walking a few blocks, visiting friends/relatives, gardening, driving, and climbing stairs. The second and third items ask about well-being and the number of days of problems due to illness. The next seven items assess the patients' ability to work, pain intensity, fatigue, stiffness, good sleep, anxiety and depression during the previous week using VAS. The maximum total score is 100. High scores indicate low functionality of the patient.

  up to 4 weeks

Study Arms (2)

Experimental: exercise

EXPERIMENTAL

Do Exercise

Behavioral: Exercise

Control

ACTIVE COMPARATOR

do nothing

Behavioral: Control (Standard treatment)

Interventions

Exercise BEHAVIORAL

The exercise program lasts 32 minutes in total. The first 6 (six) minutes of this program consists of warm-up exercises. Active exercise time is 21 (twenty-one) minutes. Relaxation exercises consist of 5 (five) minutes of relaxation exercises. exercise was accompanied by music. it consists of warm-up exercise and relaxation sections.

Experimental: exercise

Control (Standard treatment) BEHAVIORAL

do nothing

Control

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Being diagnosed with fibromyalgia according to the 2016 American College of Rheumatology criteria in the Physical Therapy and Rehabilitation unit of the University of Health Sciences Kanuni Sultan Süleyman Training and Research Hospital,
• Being between the ages of 18 and 65,
• Volunteering to participate in the study.
• Having no problem with perception
• Being diagnosed with fibromyalgia at least 6 (six) months ago.
• Not using any alternative treatment method (acupuncture, mud, etc.).

You may not qualify if:

• Cardiovascular, respiratory, metabolic and rheumatic diseases that may limit exercise;
• Diseases associated with autonomic dysfunction such as arterial hypertension, diabetes and coronary insufficiency;
• Having exercised in the last 3 months,
• Having a disease that causes problems in understanding the questionnaires
• Pregnancy or breastfeeding.
• History of surgery in the last four months.

Sponsors & Collaborators

• Istanbul Medeniyet University: lead

Study Sites (1)

İstanbul

Istanbul, Kartal, 34862, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Fibromyalgia; Somatoform Disorders; Motor Activity; Syndrome

Interventions

Exercise

Condition Hierarchy (Ancestors)

Muscular Diseases; Musculoskeletal Diseases; Rheumatic Diseases; Neuromuscular Diseases; Nervous System Diseases; Mental Disorders; Behavior; Disease; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Motor Activity; Movement; Musculoskeletal Physiological Phenomena; Musculoskeletal and Neural Physiological Phenomena

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: PREVENTION
• Intervention Model: FACTORIAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Nursing Associate Professor

Model Details: Assuming a power of 80% and an α risk of. 05, a sample size of 75 was determined to be appropriate. Considering the possibility of missing data, the study initially included 80 participants in both the experimental and control groups. A computer-based random number generator was used for group assignment, and allocation concealment was ensured by using sealed envelopes containing random numbers opened by a separate researcher. The study was completed with 40 participants in the experimental group and 40 in the control group, due to some participants withdrawing.

Study Record Dates

• First Submitted: April 25, 2025
• First Posted: May 4, 2025
• Study Start: December 21, 2023
• Primary Completion: November 23, 2024
• Study Completion: December 21, 2024
• Last Updated: May 4, 2025

Record last verified: 2025-04

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)