Physiotherapy and Reaction Time in Hemophilia

NCT06331091 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2024-04-02

No results posted yet for this study

Summary

This randomised controlled study was conducted to investigate the comprehensive physiotherapy combined with home exercises on individuals with hemophilic arthropathy in the lower extremity. There are two groups in the study: home exercises and comprehensive physiotherapy combined with home exercises. Is physiotherapy combined with home exercises superior to home exercises on joint health, bleeding frequency, reaction time, dynamic balance, muscle strength? The aim of this study is to increase the compliance of hemophilic individuals to physiotherapy and adapt home exercises to their lives with weekly sessions.

Conditions

  • Hemophilia Arthropathy

Interventions

OTHER

Home exercise

Home exercise are done at home without the supervision of a specialist.

OTHER

Manual therapy

Manual therapy is special techniques for soft tissues and joints applied by a physiotherapist.

DEVICE

Neuromuscular electrical stimulation

Home exercise are done at home without the supervision of a specialist. Manual therapy is special techniques for soft tissues and joints applied by a physiotherapist. Neuromuscular electrical stimulation is the application of electrical current to the muscle through special electrodes in order to increase muscle strength. Supervised exercise is done under the supervision of a physiotherapist.

OTHER

Supervised exercise

Supervised exercise is done under the supervision of a physiotherapist.

Sponsors & Collaborators

  • Yuzuncu Yıl University

    lead OTHER

Principal Investigators

  • Ayse Merve Tat, Asst. Prof. · Van Yüzüncü Yıl University, Faculty of Health Science

  • Necati Muhammed Tat · Van Yüzüncü Yıl University, Faculty of Health Science

  • Serbay Şekeröz, Asst. Prof. · Van Yüzüncü Yıl University, Faculty of Health Science

  • Meryem M Büke, Asst. Prof. · Van Yüzüncü Yıl University, Faculty of Health Science

  • Kamuran M Karaman, Prof. · Van Yüzüncü Yıl University, Faculty of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
32 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-12-10
Primary Completion
2024-01-19
Completion
2024-01-19

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06331091 on ClinicalTrials.gov