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Enrolling by invitation NCT07552103

The Effect of Thyroid Dysfunction

Observational Thyroid Dysfunction

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: Thyroid Dysfunction. Basic parameters: 18 years — 55 years · Female.
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 Effect of Thyroid Dysfunction on Pain, Symptoms, Attitudes, Fatigue, Foot Parameters, Muscle Strength, and Lower Limb Performance in Women With a Menstrual Cycle: A Cross-Sectional Comparative Study

Overview

The aim of this study is to investigate the effect of thyroid dysfunction on pain, symptoms, attitudes, fatigue, foot parameters, muscle strength, and lower extremity performance in women with a menstrual cycle, and to compare these findings with those of healthy controls.

Primary outcome measures

  • Foot Function Index [Time frame: At baseline (Day 1)]
  • Foot Posture Index-6 [Time frame: At baseline (Day 1)]
  • Sit-to-Stand Test [Time frame: At baseline (Day 1)]
  • Trunk Flexor Endurance Test [Time frame: At baseline (Day 1)]
  • Trunk Lateral Flexor Endurance Test [Time frame: At baseline (Day 1)]
  • Longitudinal Arch Measurement [Time frame: At baseline (Day 1)]
Secondary outcome measures (5)
  • Menstrual Symptom Scale [Time frame: At baseline (Day 1)]
  • Visual Analog Scale [Time frame: At baseline (Day 1)]
  • Menstrual Attitude Scale [Time frame: At baseline (Day 1)]
  • Multidimensional Fatigue Inventory-20 [Time frame: At baseline (Day 1)]
  • Time up and go test [Time frame: At baseline (Day 1)]

Eligibility criteria

Inclusion criteria

  • Be between the ages of 18 and 55
  • Be female
  • Be able to communicate in Turkish
  • Be willing to participate in the study
  • Have signed the informed consent form
  • Have a menstrual cycle

Exclusion criteria

  • Diagnosed with severe cognitive impairment or dementia
  • Having an active psychiatric diagnosis
  • Having undergone any surgery in the past year
  • Having any rheumatic, neurological, or cancer-related condition
  • Using a walking aid
  • Having a cardiopulmonary condition that could cause significant functional limitations

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

Healthy volunteers: Yes

Study design

Observational model
Case-control

Study locations

Turkey (Türkiye) · 1 center
  • Usak Training and Research Hospital, Endocrinology Outpatient Clinic — Uşak

Identifiers

NCT: NCT07552103 · Thyroid Dysfunction

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗