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Recruiting NCT06696274

Kinesiophobia, Pain, Balance, Quality of Life and Mental Status in Hemodialysis Patients

— Observational Hemodialysis End Stage Renal Disease (ESRD)

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: Hemodialysis, End Stage Renal Disease (ESRD). Basic parameters: from 18 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 →

Unsure about the terms? Read our patient guide →

Official title

Investigation of the Relationship Between Kinesiophobia and Pain, Balance, Quality of Life and Mental Status in Hemodialysis Patients

Overview

The aim of our study was to investigate the relationship between kinesiophobia and pain, balance, physical performance, quality of life and mental status in patients receiving hemodialysis.

Primary outcome measures

  • Kinesiophobia [Time frame: Day 1]
  • Pain [Time frame: Day 1]
  • Balance [Time frame: Day 1]
  • Physical performance [Time frame: Day 1]
Secondary outcome measures (3)
  • Quality of life [Time frame: Day 1]
  • Mental health [Time frame: Day 1]
  • Comorbidity level [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Patients with end stage renal disease receiving hemodialysis
  • Receiving hemodialysis for more than 3 months
  • Being clinically stable
  • Volunteering to participate in this stud

Exclusion criteria

-Having musculoskeletal disorders that may affect physical performance

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: NCT06696274 · 2024-12/101

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗