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Comparison of the Effects of MAT Pilates and MIHA Combined Exercise Programs on Pain, Quality of Life, Anxiety, and Endurance in Patients With Nonspecific Back Pain

NCT ID: NCT07286760

Last Updated: 2025-12-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-01

Study Completion Date

2025-12-25

Brief Summary

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Comparison of the Effects of MAT Pilates and MIHA Combined Exercise Programs on Pain, Quality of Life, Anxiety, and Endurance in Patients with Nonspecific Back Pain

Detailed Description

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Conditions

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Low Back Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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MIHA Combined Exercise Programs

Group Type EXPERIMENTAL

MIHA Combined Exercise Programs

Intervention Type OTHER

MIHA Combined Exercise Programs

MAT Pilates

Group Type ACTIVE_COMPARATOR

MAT Pilates

Intervention Type OTHER

MAT Pilates

Interventions

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MIHA Combined Exercise Programs

MIHA Combined Exercise Programs

Intervention Type OTHER

MAT Pilates

MAT Pilates

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Being between 25 and 45 years of age Having had back pain for the last 3 months The back pain not being due to a structural, traumatic, infectious, or tumor-related cause (i.e., no specific cause has been identified) Not having any serious cardiovascular, neurological, or orthopedic conditions that would prevent participation in a physical exercise program Not having participated in a regular physical exercise program in the past 6 months Not having any contraindications to the use of a wearable EMS device (e.g., not having a pacemaker)

Exclusion Criteria

The back pain is associated with a specific pathology (e.g., spinal stenosis, fracture, tumor, infection, etc.) Being within the first 6 months of pregnancy or postpartum History of neurological disease (e.g., multiple sclerosis, peripheral neuropathy, spinal cord injury, etc.) Having a pacemaker or other electronic device in the body Pre-existing intolerance to EMS
Minimum Eligible Age

25 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul Medipol University Hospital

OTHER

Sponsor Role lead

Responsible Party

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hazal genc

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hazal GENÇ

Istanbul, None Selected, Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Hazal GENÇ

Role: CONTACT

[email protected]
05413204291

Other Identifiers

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E-78097791-020-4745

Identifier Type: -

Identifier Source: org_study_id