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Effect of Combined Interventions on Pressure Pain Threshold

Effect of End-range Mobilization in Addition to Conservative Therapy on Decrease of Pressure Pain Threshold

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04312035
Enrollment
60
Registered
2020-03-17
Start date
2020-03-04
Completion date
2020-03-04
Last updated
2020-03-17

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

Conditions

Osteo Arthritis Knee

Keywords

Musculoskeletal Manipulations, Osteoarthritis, Knee, Pain Threshold, Conservative Treatment

Brief summary

The effect of mobilizations on decrease of peripheral and central sensitivity has been proven in KOA. Furthermore, the effect of conservative therapy has also been proven in the increase of pain threshold in KOA. However, no study has investigated the effect of these interventions combined till date in KOA. The aim of the present study is to investigate the short-term and long-term effect of end-range mobilization in addition to conservative therapy on decrease of pressure pain threshold in KOA.

Detailed description

The positive effect of different manual mobilizations have been proven in the management of knee osteoarthritis (KOA). Pressure pain threshold, as a measure of somatosensory function, is a well-applied measurement technique for the pain perception in KOA. The effect of mobilizations on decrease of peripheral and central sensitivity has been proven in KOA. Furthermore, few studies has revealed the effect of conservative therapy as an effective intervention in the increase of pain threshold. However, no study has investigated the effect of these interventions combined till date in KOA, which could give a long-lasting effect in the decrease of sensitization in KOA. Therefore, the aim of the present study is to investigate the short-term and long-term effect of end-range mobilization in addition to conservative therapy on decrease of pressure pain threshold in KOA.

Interventions

accessory technique applied on the tibiofemoral joint with the aim of increasing extensibility of the periarticular tissues

accessory technique applied on the tibiofemoral joint with the aim of alleviating pain

PROCEDUREControl

hands-on cutaneous technique

Sponsors

University of Pecs
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
60 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* clinical classification criteria of knee osteoarthritis according to the American College of Rheumatology * categorization as End of Range Problem based on Maitland manual therapy * unilateral/bilateral moderate-to-severe symptomatic tibiofemoral KOA with radiographic evidence of Kellgren-Lawrence scale 2 or 3 * pain during weight-bearing activities at least within 6 months * at least 90° knee flexion * sufficient mental status

Exclusion criteria

* acute inflammation of the knee * total knee replacement in the opposite side * class II. obesity (body mass index\>35kg/m2) * severe degenerative lumbar spine disease (e.g. spondylolisthesis) * systemic inflammatory arthritic or neurological condition * physiotherapy/balneotherapy attendance or manual therapy within 3 months * intraarticular injections in the prior 12 months * use of walking aid * contraindication for manual therapy * complex regional pain syndrome * cognitive impairment

Design outcomes

Primary

MeasureTime frameDescription
change of peripheral sensitivityfollowing 3-week rehabilitationperipheral sensitivity (pressure pain threshold) assessed at the local knee

Secondary

MeasureTime frameDescription
change of general pain intensityfollowing 3-week rehabilitationgeneral pain intensity from the previous week using the Visual Analogue Scale
change of Timed Up and Go testfollowing 3-week rehabilitationshort test for measuring physical performance
change of pain intensity during physical performancefollowing 3-week rehabilitationpain intensity measured during the previously mentioned physical performance test using the 0-10 Numerating Pain Rating Scale, where 0 indicate no pain and 10 indicate worst imaginable pain
change of central sensitivityfollowing 3-week rehabilitationcentral sensitivity (pressure pain threshold) assessed at the ipsilateral m. extensor carpi radialis longus
degree of knee flexion during passive movement at the onset of knee painfollowing 3-week rehabilitationmeasurement of degree of knee flexion during passive movement at the onset of knee pain
strength of resistance of passive knee flexion at the onset of knee painfollowing 3-week rehabilitationmeasurement of strength of resistance arising from the anterior located tissues around the knee during passive knee flexion at the onset of pain
change of pain during physical performancefollowing 3-monthpain intensity measured during the previously mentioned physical performance test using the 0-10 Numerating Pain Rating Scale, where 0 indicate no pain and 10 indicate worst imaginable pain

Countries

Hungary

Outcome results

None listed

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