Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06848608

Comparison of the Effects of Yoga and Conventional Physiotherapy Programs on Fatigue, Pulmonary Functions and Exercise Capacity in Patients With Sarcoidosis

Led by Saglik Bilimleri Universitesi · Updated on 2025-02-27

32

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

S

Saglik Bilimleri Universitesi

Lead Sponsor

I

Istanbul Saglik Bilimleri University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Sarcoidosis is a complex disease that can affect many organs and systems, most commonly the lungs, leading to reduced lung capacity, muscle weakness, and symptoms like shortness of breath and fatigue. It mostly occurs in young and middle-aged adults and impacts quality of life through physical and emotional challenges, including anxiety and depression. This research aims to compare the effects of yogic techniques and conventional physiotherapy on lung function, exercise capacity, fatigue, mental health, sleep, and overall quality of life in patients with sarcoidosis at various stages. Participants will be randomly assigned to either a conventional physiotherapy program or a yoga program, both supervised by a physiotherapist. Each program involves two days per week of group-based tele-rehabilitation and three days of home exercises tracked with a diary over 8 weeks. The physiotherapy group will perform strengthening and breathing exercises, including resistance training and thoracic expansion, while the yoga group will practice pranayama breathing techniques and yoga postures. Both groups will also engage in aerobic walking exercises three days per week. During the study, participants will undergo assessments at the start and after 8 weeks, including lung function tests, exercise capacity tests, fatigue and dyspnea evaluations, mental health scales, sleep quality, and quality of life questionnaires. The research team will monitor these measures to understand the effects of each program. The total participation time is 8 weeks, with close supervision and standardized rehabilitation exercises to support patient well-being and gather comprehensive data.

CONDITIONS

Brief Title

Comparison of the Effects of Yoga and Conventional Physiotherapy Programs in Sarcoidosis

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with sarcoidosis by a physician at Stage II, III, or IV
  • Lung involvement due to sarcoidosis
  • Experiencing fatigue with a Fatigue Assessment Scale score of 22 or higher
  • No use of immunosuppressive drugs in the past 1 year
  • No use of antidepressant medications in the past 6 months
  • Age between 18 and 75 years
Not Eligible

You will not qualify if you...

  • Cognitive impairment that prevents communication
  • Anemia
  • Uveitis
  • Diabetes
  • Pregnancy
  • Major cardiovascular diseases
  • Bone fractures
  • Osteoporosis
  • Neurological or orthopedic diseases affecting treatment
  • Being in an exacerbation phase of sarcoidosis
  • Presence of tumors

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 8 weeks

Participants receive either a conventional physiotherapy program or a yoga program designed to improve pulmonary functions, exercise capacity, and reduce fatigue. Both programs include aerobic walking and are delivered with supervised tele-rehabilitation twice a week plus exercises on other days for a total of 8 weeks.

2 supervised group sessions per week plus 3 additional exercise days with diary monitoring

Trial Site Locations

Total: 1 location

1

Süreyyapaşa Chest Diseases and Chest Surgery Training and Research Hospital

Istanbul, Maltepe, Turkey (Türkiye), 34844

Actively Recruiting

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Research Team

Ş

Şeyda YILDIZ, PhD(c), PT

Z

Zuhal D TAKİNACI, Asst Prof, PT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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