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Enrolling by invitation NCT07665086

The Role of Isometric in Individuals With Rheumatoid Arthritis

No phase Interventional Isometric Exercise Pain Oxygenation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Exercise.
Who it may be relevant to
Registry conditions: Isometric Exercise, Pain, Oxygenation. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Role of Isometric Exercise on Pain Modulation and Muscle Oxygenation in Individuals With Rheumatoid Arthritis

Overview

The aim of this study is to investigate the acute effects of isometric exercise on pain modulation and muscle oxygenation in individuals with rheumatoid arthritis.

Interventions

  • Other Exercise
    To determine isometric exercise intensity, a maximum repetition will be calculated individually using a handheld dynamometer. One maximum repetition will be defined as the highest value among the trials where participants squeezed the handheld dynamometer as hard as possible for 5 seconds. The average of 3 repetitions will be taken to determine one maximum repetition, with a 1-2 minute rest period between each repetition. 30% of one maximum repetition will be determined. The exercise will begin

Primary outcome measures

  • Pain Tolerance Assessment [Time frame: Day 1]
  • Pressure Pain Threshold Assessment [Time frame: Day 1]
  • Temporal Summation Measurement [Time frame: Day 1]
  • Conditional Pain Modulation Assessment [Time frame: Day 1]
  • Visual Analog Scale (VAS) - Pain [Time frame: Day 1]
Secondary outcome measures (6)
  • Quantitative Sensory Tests [Time frame: Day 1]
  • Muscle Oxygen Saturation Measurement [Time frame: Day 1]
  • The Body Awareness Questionnaire [Time frame: Day 1]
  • ABILHAND Rheumatoid Arthritis Hand Function Questionnaire [Time frame: Day 1]
  • Pain Catastrophizing Scale [Time frame: Day 1]
  • The International Physical Activity Questionnaire - Short Form [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Eligibility Criteria:
  • Diagnosis of rheumatoid arthritis
  • Being between 18-65 years of age
  • Volunteering to participate in the study

Exclusion criteria

  • Having a neurological disease
  • Having pulmonary or cardiovascular problems that may affect daily living activities
  • Sensory system disorders
  • Previous upper extremity surgery
  • Having cognitive impairment
  • Having an accompanying rheumatic disease
  • Fracture, dislocation, or surgical intervention in the hand/wrist region within the last 6 months
  • Communication limitations that prevent following the study protocol
  • Having an exercise history in the last six months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Prevention

Study locations

Turkey (Türkiye) · 1 center
  • Pamukkale University — Denizli

Identifiers

NCT: NCT07665086 · Isometric Exercise

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗