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MAT Pilates and MIHA Combined Exercise Programs in Patients With Nonspecific Back Pain

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07286760
Enrollment
40
Registered
2025-12-16
Start date
2025-08-01
Completion date
2025-12-25
Last updated
2026-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

exercise

Brief summary

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

Interventions

OTHERMIHA Combined Exercise Programs

MIHA Combined Exercise Programs

MAT Pilates

Sponsors

Istanbul Medipol University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pain Assessment12 weeksAn algometer will be used to measure pain levels. We have identified three muscle groups for the algometer: Gluteus Medius, Erector Spinae, and Quadratus Lumborum. A low level indicates greater sensitivity and weakness.
Quality of Life Assessment12 weeksQuality of life will be assessed using the Oswestry Disability Index. It is used to evaluate the effect of the MAT Pilates and EMS-assisted exercise programs applied in the study on daily living activities. The lower the total score, the less the disability.The Oswestry Disability Index (ODI) ranges from 0 (no disability) to 100 (maximum disability), with higher scores reflecting increased functional impairment.
Anxiety Assessment12 weeksIndividuals' anxiety levels are assessed using the Beck Anxiety Scale. This assessment aims to compare individuals' anxiety levels before and after intervention. A high score on the Beck Anxiety Scale indicates a higher level of anxiety. The Beck Anxiety Inventory (BAI) is scored from 0 to 63, with higher scores indicating greater levels of anxiety.
Endurance Assessment12 weeks: Individual endurance is assessed using three movements: the Plank, Bridge Movement, and V-Sit position. These selected movements target the anterior, posterior, and lateral core muscle groups, enabling an assessment of overall endurance.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026