🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07394361
Enrolling by invitation Not applicable

The Effect of Clinical Pilates Training on Fatigue, Emotional State, Functional Capacity, Sleep and Quality of Life in Women With Systemic Lupus Erythematosus

NCT07394361 · tracked via the Priya Life Science Turkey tracker
Sponsor
Emir İbrahim IŞIK
Phase
Not applicable
Started
2025-03-07
Last updated
2026-02-06

Condition(s) studied

Lupus Erythematosus, Systemic

Investigational drug(s) / intervention(s)

Clinical Pilates TrainingHome exercise program

Clinical Pilates Training: Warm-up (5 min) Segmental extremity movements Centering Roll down Pilates exercises (35 min) One leg stretch Double leg stretch Shoulder bridge Chest lift Hundreds Side band Arm opening Cobra Swimming Push-up Cool-down (5 min) Cat stretching Camel stretching Relaxation exercises

Home exercise program: This program will consist of stretching, relaxation, and strengthening exercises, to be performed three days a week for a period of eight weeks.

Study summary

Systemic lupus erythematosus (SLE) is a chronic, autoimmune, inflammatory disease with the potential to affect any organ in the body. The most frequently affected anatomical regions include the skin, joints, pleura, pericardium, kidneys and the central nervous system.

All systemic conditions observed in SLE cause functional deficiencies in daily life, fatigue, anxiety and depression, pain, sleep quality disorders, cognitive effects, cosmetic problems, social isolation, and all these characteristics negatively affect the quality of life of an individual with SLE.

The aim of this study is to investigate the effects of clinical pilates exercises on pain, fatigue, functional capacity, flexibility, emotional state, sleep and quality of life in patients with SLE.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
55 Years
Healthy volunteers
No
Inclusion Criteria: * being a woman between the 18 Years to 65 Years , * meeting the American College of Rheumatology SLE diagnostic criteria, * having low disease activity (SLEDAI ≤4), * agreeing to participate in the study Exclusion Criteria: * presence of malignancy, pregnancy, change of treatment within the last 3 months, * use of steroids equivalent to \>16 mg prednisolone for the last 3 months, - - * have other rheumatic diseases, * have a regular exercise habit (physical activity more than two times a week), * have a disease that restricts physical activity (such as neurological disorder, orthopedic disorder, cognitive disorder, immobility), * have serious heart, lung or kidney involvement, * uncontrolled hypertension, * severe anemia (hb \<8 g/dL), * having undergone orthopedic surgery in the last 6 months

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Cukurova University Adana Saricam

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07394361 on ClinicalTrials.gov ↗ ← All trials in Turkey