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Neuromuscular Electrical Stimulation and Ultrasound Therapies , Knee Osteoarthritis

Recep Tayyip Erdogan University Medical School

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03727256
Enrollment
103
Registered
2018-11-01
Start date
2017-02-01
Completion date
2017-10-30
Last updated
2018-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

knee osteoarthritis, neuromuscular electrical stimulation, ultrasound therapy

Brief summary

To determine the effects of ultrasound therapy and neuromuscular electrical stimulation on the muscle architecture and functional capacity of patients with knee osteoarthritis.

Detailed description

All participants who were satisfied with the inclusion criteria were randomly assigned to one of two study groups: Group 1- ultrasound therapy group; Group 2 - the neuromuscular electrical stimulation group. Group allocation was randomized in two blocks of 30 sealed envelopes without external marks, which were mixed and numbered from 1 to 30, containing a piece of paper with the group allocation. The researchers responsible for outcome measures and ultrasonograhic measurements were blinded to the patients' diagnosis or intervention.

Interventions

OTHERultrasound therapy

Group 1, ultrasound therapy ;1 watt/cm² dose, 1 MHz, 5 minutes

Group 2, neuromuscular electrical stimulation application;20 mins/session

Sponsors

Recep Tayyip Erdogan University Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
50 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Inclusion Criteria: Clinical diagnosis of knee osteoarthritis 2.

Exclusion criteria

Cardiovascular diseases Inflammatory diseases Infectious diseases Lower extremity weakness Tumoral diseases Knee surgery in the past six months Intra-articular injection in the past six months

Design outcomes

Primary

MeasureTime frameDescription
Visual analog scale3 weeksPain was assessed using a 0 to 10 visual analogue pain scale, with 0 meaning 'no pain' and 10 meaning 'excruciating pain'.
Western Ontario and McMaster Universities Arthritis Index3 weeksThe WOMAC (Westren Ontario and McMaster Universities) index is used to assess patients with osteoarthritis of the hip or knee using 24 parameters.To assess pain, stiffness, and physical function in patients with hip and / or knee osteoarthritis, Minimum total score: 0, maximum total score: 96.Disability scores increase as Womac osteoarthritis index scores increase.
15 meter walking test3 weeksThe patients were asked to walk as fast as possible along a level, unobstructed corridor on the command go. The patients stood before the starting line. A hand-held stopwatch was started as the subjects passed a predetermined start mark and stopped as they passed a second mark 15meter from the start mark.Walking duration was determined as second before and after treatment
Muscle measurements were made before and after treatment.3 weeksUltrasonography was used to measure muscle thickness, pennation angle and fascicle length. Muscle thickness was measured as the mean distance between the superficial and deep aponeurosis at both image muscles. The distance between the intersection composed of the superficial aponeurosis and muscle fascicle, and the intersection composed of the deep aponeurosis and muscle fascicle was defined as muscle fascicle length. The results was measured as millimeter.The angle between the muscle fascicle and deep aponeurosis was defined as Pennation angle.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026