The Effects of Online Mat Pilates and Face-to-Face Equipment-Based Pilates on Pain, Kinesiophobia, and Balance in Individuals With Non-Specific Low Back Pain

NCT ID: NCT06946966

Last Updated: 2025-08-12

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

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-17

Study Completion Date

2025-08-11

Brief Summary

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Non-specific low back pain (NSLBP) is a common musculoskeletal condition that affects a significant portion of the population and often leads to limitations in daily activities, reduced quality of life, and increased levels of kinesiophobi

Detailed Description

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compare the effects of online mat Pilates and face-to-face equipment-based Pilates on pain, kinesiophobia, and balance in individuals with NSLBP. While both methods emphasize neuromuscular control and alignment, differences in delivery modes and equipment usage may influence outcomes.

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

Investigators

Study Groups

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Reformer Pilates

Reformer Pilates

Group Type EXPERIMENTAL

Reformer Pilates

Intervention Type OTHER

Reformer Pilates

Pilates control

Pilates control

Group Type ACTIVE_COMPARATOR

Pilates control

Intervention Type OTHER

Pilates control

pilates online pilates

online pilates

Group Type ACTIVE_COMPARATOR

pilates online pilates

Intervention Type OTHER

pilates online pilates

Interventions

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Reformer Pilates

Reformer Pilates

Intervention Type OTHER

Pilates control

Pilates control

Intervention Type OTHER

pilates online pilates

pilates online pilates

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Aged between 18 and 60 years
* Non-specific low back pain for more than 12 weeks
* No clear pathological diagnosis
* Physically and cognitively capable of performing the exercises
* Pain level between 3 and 7 on the Visual Analog Scale (VAS)

Exclusion Criteria

* Pregnancy
* Spinal surgery in the last 6 months
* Neurological or chronic systemic diseases
* Movement restriction due to severe pain
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

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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Bahceşehir University Health Center

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2024-04/02

Identifier Type: -

Identifier Source: org_study_id

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