Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06166199

Effects of High-intensity Interval Training in Patients With Systemic Lupus Erythematosus

Led by Karolinska Institutet · Updated on 2023-12-12

40

Participants Needed

1

Research Sites

217 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

S

Swedish Rheumatism Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

The aim of this study is to evaluate the safety and effects of high-intensity interval training (HIIT) combined with resistance training in patients with systemic lupus erythematosus

CONDITIONS

Official Title

Effects of High-intensity Interval Training in Patients With Systemic Lupus Erythematosus

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Diagnosed with systemic lupus erythematosus (SLE) based on accepted criteria or clinical diagnosis
  • Low to moderate disease activity (score of 5 or less on clinical SLEDAI-2K)
  • Low or minimal organ damage (score of 3 or less on SLICC/ACR Damage Index)
  • Stable medication treatment
  • Able to perform a maximal ergometer cycle exercise test
  • Able to read and understand Swedish
Not Eligible

You will not qualify if you...

  • History or symptoms of serious cardiovascular, pulmonary, or cerebrovascular diseases within the past year
  • Chronic kidney disease
  • Absolute contraindications for maximal exercise testing according to American Heart Association
  • Unable to perform maximal ergometer cycle exercise test due to disease
  • Conditions strongly limiting ability to exercise or where exercise is not recommended
  • Regular aerobic or strength training more than once weekly
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Carina Boström

Stockholm, Huddinge, Sweden, 141 83

Actively Recruiting

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Research Team

C

Carina M Boström, Dr

CONTACT

I

Ioannis Parodis, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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