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Recruiting NCT06696287

The 6-minute Pegboard and Ring Test in Patients with Fibromyalgia Syndrome

Observational Fibromyalgia

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Fibromyalgia. 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

Validity and Reliability of the the 6-minute Pegboard and Ring Test in Patients with Fibromyalgia Syndrome

Overview

The aim of our study is to investigate the validity and reliability of the 6-minute pegboard and ring test in patients with fibromyalgia syndrome.

Primary outcome measures

  • Arm exercise capacity [Time frame: 10 minutes]
  • Functional exercise capacity [Time frame: 20 minutes]
  • Hand grip strength [Time frame: 5 minutes]
Secondary outcome measures (2)
  • Activities of daily living [Time frame: 10 minutes]
  • Functional status/limitation [Time frame: 5 minutes]

Eligibility criteria

Inclusion criteria

  • Being diagnosed with fibromyalgia syndrome
  • Being aged 18-65
  • Stable use of medication for at least 3 months or longer
  • Volunteering to participate in the study

Exclusion criteria

  • Having a musculoskeletal problem that would prevent being tested
  • Having cardiopulmonary and neurological disease
  • Malignancy
  • Pregnancy

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

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

Turkey (Türkiye) · 1 center
  • Kirsehir Ahi Evran University — Kırşehir

Identifiers

NCT: NCT06696287 · 2024-13/112

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗