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Completed

NCT Number: NCT07339410

Physiotherapy to Improve Balance and Walking Capacity in Hemophilia

Introduction: Hemarthrosis is the most common type of bleeding with 70-80% in patient with hemophilia (PwH) and the majority of hemarthrosis occurs in the knee and ankle joints. Recurrent hemarthrosis may cause pain, limited range of motion (ROM), atrophy, swelling, crepitus, and decreased proprioceptive sensation and ultimately causes hemophilic arthropathy. Preventing hemarthrosis and treating arthropathy symptoms in PwH may improve static and dynamic balance and walking capacity. The aim of this study was to investigate the effects of manual therapy and structured exercises on joint health, activity pain, walking capacity and static and dynamic balance.

Method: Thirty-five AwH were randomly assigned to two groups using the computerised simple randomization method: the control group (CG) and the physiotherapy group (PG). The sample sizes for the CG and PG are 17 and 18, respectively. Hemophilia type and severity, treatment regime (prophylaxis or on-demand), age, height and weight were recorded. Joint health was assessed with Hemophilia Joint Health Score (HJHS) version 2.1 by a hemophilia specialist physiotherapist. Activity pain was assessed with Numeric Pain Scale (NPS). Walking capacity was evaluated 6 Minute Walking Test (6MWT). Postural balance (static and dynamic balance) were evaluated with the Pro-kin Technobody Posturographic Platform (Pro-kin 212, Technobody s.r.l, Dalmine, 21044 Bergamo, Italy). Static stability test was used for static balance assessment. Dynamic balance was evaluated with the Limits of Stability (LoS) test. The PG received 12 physiotherapy sessions twice a week for 6 weeks. The physiotherapy intervention consisted of manual therapy and a structured, progressive exercise program. The CG continued with their routine hemophilia care.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Severe or moderate hemophilia A or B
  • Aged 18-65
  • Having at least 3 points from at least one of the knee and ankle index joints in the Hemophilia Joint Health Score
  • Volunteering to attend physiotherapy sessions regularly

Exclusion criteria

  • Receiving physiotherapy or undergone surgery on lower extremity within the last 6 months
  • Having neurological or cognitive disease
  • Having visual and vestibular system pathologies

Treatment and study plan

Physiotherapy

Other

The physiotherapy intervention applied in this study included manual therapy and a structured and progressive exercise program.

Primary outcomes

  1. Postural balance

    Time frame: From enrollment to the end of treatment at 6 weeks

    Static and dynamic postural balance were evaluated with the Pro-kin Technobody Posturographic Platform (Pro-kin 212, Technobody s.r.l, Dalmine, 21044 Bergamo, Italy).

  2. Walking capacity

    Time frame: From enrollment to the end of treatment at 6 weeks

    Walking capacity was evaluated with 6 Minute Walking Test.

Secondary outcomes

  1. Activity pain

    Time frame: From enrollment to the end of treatment at 6 weeks

    Activity pain was evaluated with Numeric Pain Scale

  2. Joint health

    Time frame: From enrollment to the end of treatment at 6 weeks

    Joint health was evaluated with Hemophilia Joint Health Score

Sponsors and collaborators

Lead sponsor

Yuzuncu Yil University

Other

Registry information

Official study title

Effects of Manual Therapy and Structured Exercises on Postural Balance and Walking Capacity in Adults With Hemophilia

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Jan 14, 2026
Registry last updated
Jan 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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