Skip to main content
Clinical Trials/NCT05947110
NCT05947110CompletedNot Applicable

How Effective is the Plyometric-based Hydro-kinesio Therapy for Pain, Muscle Strength, Postural Control, and Functional Performance in Children With Hemophilic Knee Arthropathy?

Cairo University1 site in 1 country48 target enrollmentStarted: September 5, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
48
Locations
1
Primary Endpoint
Postural control

Study Overview

Brief Summary

This study was designed to assess the effect of an 8-week plyometric-based hydro-kinesio therapy (Plyo-HKT) on pain, muscle strength, postural control, and functional performance in a convenience sample of children with hemophilic knee arthropathy (HKA). Forty-eight patients with HKA were randomly allocated to the Plyo-HKT group (n = 24, received the plyometric-based hydro-kinesio therapy program, twice/week, over 8 weeks) or the control group (n = 24, received standard exercise program). Both groups were assessed for pain, muscle strength, postural control, and functional performance pre and post-treatment.

Detailed Description

Forty-eight boys with moderate hemophilia-A were recruited from the hematology clinics of three large referral hospitals in Riyadh, Saudi Arabia. The study included patients who were 8-16 years old, had factor VIII replacement prophylaxis, were clinically-stable cases, had unilateral knee hemarthrosis, had grade II or III knee arthropathy, had muscle strength of grade three, and if they were able to walk independently. Patients who had enduring disabling pain, fixed deformities, a history of musculoskeletal surgery, visual and/or vestibular deficits, or bleeding episodes within two weeks before enrollment were excluded.

Outcome measures

Pain: Pain during rest and/or movement was assessed using the Numerical Pain Rating Scale.

Muscle strength: The peak concentric torque of the quadriceps and hamstring muscles was measured through an Isokinetic Dynamometer.

Postural control: The directional dynamic limit of stability (forward, backward, affected, and non-affected) and overall limit of stability were assessed using the Biodex balance system.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

This was a single-blind protocol. The researcher who collected the data was blinded to the treatment allocation.

Eligibility Criteria

Ages
8 Years to 16 Years (Child)
Sex
Male
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Eight and 16 years.
  • •Had factor VIII replacement prophylaxis.
  • •Clinically-stable.
  • •Unilateral knee involvement.
  • •Knee arthropathy of grade II or III per the Arnold-Hilgartner radiographic classification.
  • •Muscle strength of grade 3 in lower limb muscles.
  • •Use of no pain medication for one month prior to enrollment.
  • •Walking independently.

Exclusion Criteria

  • •Enduring disabling pain
  • •Fixed deformities.
  • •History of musculoskeletal surgery.
  • •Visual or vestibular deficits.
  • •Engagement in regular exercises.
  • •Bleeding episodes within two weeks prior to enrolment.

Arms & Interventions

Plyo-HKT group

Experimental

Participants in this group received the Plyo-HKT program

Intervention: Plyometric-based hydro-kinesio therapy (Other)

Control group

Active Comparator

Participants in this group received the standard exercise program.

Intervention: Standard exercise therapy (Other)

Outcomes

Primary Outcomes

Postural control

Time Frame: 2 months

The capacity to control and move the center of gravity in various directions across the base of support was assessed utilizing the Biodex balance system. Values are expressed as accuracy % and higher scores mean better balance capability.

Pain intensity

Time Frame: 2 months

Participants reported how much they feel pain during rest and/or movement on the 0-10 Numerical Pain Rating Scale, where 0 represents "no pain" and 10 indicates the "worst possible pain".

Muscle strength

Time Frame: 2 months

Indicated by the peak concentric torque of the quadriceps and hamstring muscles (Nm). It was measured using an Isokinetic Dynamometer.

Secondary Outcomes

  • Functional independence(2 months)
  • Six-minute walk test(2 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ragab Kamal Elnaggar

Associate Professor

Cairo University

Study Sites (1)

Loading locations...

Similar Trials