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Effects of Various Types of Ultrasound Therapy in Hip Osteoarthritis

Not Applicable
Conditions
Hip Osteoarthritis
Registration Number
NCT03952221
Lead Sponsor
Petz Aladar County Teaching Hospital
Brief Summary

This study evaluates the effects of various types of ultrasound therapy: continuous, pulsed, sham ultrasound and ultrasound combined with electrotherapy in patients with hip osteoarthritis. Beside ultrasound therapy, patients received usual physiotherapy (balneotherapy, exercise and massage) either.

Detailed Description

During ultrasound therapy electrical energy is converted into mechanical energy and heat. It has physical, chemical and biologic effects, like thermal effect, micro-massage, increased tissue metabolism, capillary permeability and tissue healing. Continuous or pulsed forms can be applied.

As pulsed ultrasound therapy has no thermal effect, greater intensity can be used. It can alleviate acute pain and inflammation. Continuous ultrasound is usually used in chronic musculoskeletal diseases, in case of limitation of joint motion because its thermal effect.

Ultrasound can be combined with electrotherapy, when the effects of the two modalities are summed up.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  • patients over 18 years of age with moderate hip osteoarthritis (radiologically Kellgren- Laurence II-III. stage)
  • chronic hip pain (for at least 8 weeks)
  • pain intensity is ≥ 50mm on a Visual Analogue Scale
  • no physiotherapy or local injection (steroid, hialuronic acid) within 3 months before starting the study
Exclusion Criteria
  • acute hip pain (duration is less than 8 weeks)
  • steroid, hialuronic acid injection into the hip joint within 3 months
  • physiotherapy of the hip within 3 months
  • inflammatory hip osteoarthritis
  • infection
  • fever
  • tumour
  • epilepsy
  • pregnancy
  • untreated hypertension
  • heart failure (NYHA II-IV. stage)
  • inflammatory rheumatic diseases
  • hip arthroplasty
  • pacemaker or intracardiac device
  • severe osteoporosis
  • osteomyelitis

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
change in functionWeek 0 and Week 12

change from baseline physical function measured by the 6-minute walking test at Week 12. The test measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface. Patients can walk at a self chosen walking speed, can have a rest or can use a walking aid. The accomplished distance is the total distance at the end of the 6 minutes.

change in quality of lifeWeek 0 and Week 12

change from baseline quality of life (36-Item Short Form Health Survey /SF-36/) at week 12. It consists of eight scaled scores (vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, mental health), which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more the disability, i.e. a score of zero is equivalent to maximum disability.

change in severity of pain at restWeek 0 and Week 12

change from baseline severity of pain at rest recorded on a 100 mm visual analogue scale, where 0 mm represents no pain, 100 mm represents unbearable pain.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (2)

Petz Aladár County Teaching Hospital

🇭🇺

Győr, Hungary

Zsigmondy Vilmos Harkány Spa Hospital

🇭🇺

Harkány, Hungary

Petz Aladár County Teaching Hospital
🇭🇺Győr, Hungary

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