The Effects of Progressive Clinical Pilates Exercises Applied as 2 Different Ways in Fibromyalgia

NCT ID: NCT06277596

Last Updated: 2024-04-16

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

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-10

Study Completion Date

2024-08-30

Brief Summary

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The aim of this study is to compare the effects of progressive clinical Pilates exercises applied as group under the supervision of a physiotherapist and home exercise programs on pain level, physical condition, functional status, psychosocial status and quality of life in individuals with fibromyalgia between the ages of 20-50.

Detailed Description

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After the voluntary individuals with Fibromyalgia (FM) who meet the inclusion criteria are evaluated, they will be randomly divided into two groups: exercise group and home exercise group.

The same clinical Pilates program will be applied to both groups at the same dosage. Evaluations and treatment will be applied to both groups by the same physiotherapist. Individuals will perform the exercises 10 repetitions, 3 days a week, for 6 weeks. The exercise program will be progressed as basic stabilization exercises in the first 3 weeks, advanced stabilization exercises in the last 3 weeks, as recommended in the literature, and a 30-second rest will be given between sets. For the home exercise group, all exercises will be shown and it will be ensured that they are performed correctly. Patients will be given an illustrated and descriptive exercise program brochure containing information about exercise position, number of repetitions, contraction duration, rest time between sets, frequency, and an exercise diary for exercise tracking.

Conditions

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Fibromyalgia

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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Supervise clinical Pilates group

Clinical Pilates exercises will be performed 10 repetitions, 3 days a week, for 6 weeks, under the supervision of a physiotherapist. The exercise program will be progressed as basic stabilization exercises in the first 3 weeks, advanced stabilization exercises in the last 3 weeks, as recommended in the literature, and a 30-second rest will be given between sets.

Group Type EXPERIMENTAL

Exercise

Intervention Type OTHER

Clinical Pilates exercises (basic and advanced stabilization exercises)

Clinical Pilates as home exercise

The same exercises will be shown to the home exercise group and it will be ensured that they are performed correctly. Patients will be given an illustrated and descriptive exercise program brochure containing information about exercise position, number of repetitions, contraction duration, rest time between sets, frequency, and an exercise diary for exercise tracking. In the 3rd week, new exercises will be shown to individuals. It will be applied 10 times, 3 days a week, for 6 weeks. The exercise program will be progressed as basic stabilization exercises in the first 3 weeks, advanced stabilization exercises in the last 3 weeks, as recommended in the literature, and a 30-second rest will be given between sets.

Group Type ACTIVE_COMPARATOR

Exercise

Intervention Type OTHER

Clinical Pilates exercises (basic and advanced stabilization exercises)

Interventions

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Exercise

Clinical Pilates exercises (basic and advanced stabilization exercises)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Volunteer individuals between the ages of 20-50
* Diagnosed with fibromyalgia according to the American College of Rheumatology criteria
* Pain level 3 and above according to visual analogue scale.
* Individuals who are sedentary (who have not engaged in physical activity at least 3 days a week in the last 3 months) will be included in the study.

Exclusion Criteria

* Having additional rheumatic disease
* Using NSAIDs and antidepressant drugs
* Individuals with orthopedic, neurological and cardiopulmonary diseases that prevent them from exercising
* Pregnant women
* Malignancy
* Individuals with uncontrolled systemic diseases (diabetes, systemic arterial hypertension, thyroid dysfunction, neurological, cardiorespiratory, musculoskeletal problems, etc.)
Minimum Eligible Age

20 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eastern Mediterranean University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ebru Kadıoğlu, PT

Role: PRINCIPAL_INVESTIGATOR

Eastern Mediterranean University

Sevim Oksuz, Asst.Prof.Dr

Role: STUDY_DIRECTOR

Eastern Mediterranean University

Locations

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Eastern Mediterranean University

Famagusta, , Cyprus

Site Status RECRUITING

Countries

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Cyprus

Central Contacts

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Ebru Kadıoğlu, PT

Role: CONTACT

5428734011 ext. +90

Sevim Öksüz, Asst.Prof.Dr

Role: CONTACT

5488351465 ext. +90

Facility Contacts

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Sevim Oksüz, Asst.Prof.Dr

Role: primary

5488351465 ext. +90

Other Identifiers

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ETK00-2023-0101

Identifier Type: -

Identifier Source: org_study_id

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