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Effects of a Stretching Protocol in Patients With Hip Osteoarthritis

Effects of a Stretching Protocol of Hip Flexors in Patients With Mild to Moderate Hip Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03702595
Enrollment
15
Registered
2018-10-11
Start date
2018-08-01
Completion date
2018-12-30
Last updated
2020-01-21

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

Conditions

Hip Osteoarthritis

Keywords

Hip Osteoarthritis, Manual therapy, physiotherapy

Brief summary

Hip osteoarthritis (OA) is one of the most prevalent chronic disease in the world. Clinical guidelines recommend non-pharmacological conservative treatments for the management of OA. Hip flexors seems to play an important role in the development of hip OA but there is no published studies evaluating the results of a stretching protocol of hip flexors in hip OA patients. The objective of this trial is to evaluate if a stretching protocol of hip flexors is more effective in symptoms, functional capacity , range of motion, strength, muscular length, pain threshold and anxiety and depression compared to control. For this purpose the investigators conduct a single-group, pretest-posttest clinical trial.The investigators included patients diagnosed of hip osteoarthritis Grade I-III by Scale of Kellgren and Lawrence. The variables are measured at the beginning and at the end of treatment of the control phase, and at the end of the stretching protocol phase.

Interventions

OTHERHip flexors stretching protocol

Stretching protocol of rectus femoris, vastus lateralis and iliopsoas according to Kaltenborn- Evjenth Orthopaedic Manual Therapy Concept (OMT)

Sponsors

University of Valladolid
CollaboratorOTHER
Universidad de Zaragoza
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Diagnosed medically with a X-Ray test * American College of Rheumatology Criteria

Exclusion criteria

* Secondary osteoarthritis by a traumatism, Paget disease, inflammatory or metabolic disease, congenital diseases etc. * Vascular or neurological disease. * Musculoskeletal pathologies in lumbar spine, pelvis or lower limbs * Grade IV in Kellgren and Laurence Scale

Design outcomes

Primary

MeasureTime frameDescription
Changes from baseline in pain intensity3 weeksVisual Analogic Scale

Secondary

MeasureTime frameDescription
Functional Capacity3 weeksThe investigators measure the functional capacity with Timed Up and Go test (TUG)
WOMAC questionnaire3 weeksWOMAC questionnaire
Hip Range of Motion3 weeksDigital inclinometer according to Pua et al., 2008
Muscular strength3 weeksThe investigators measure the hip strength with a hand held dynamometer (Lafayette)
Pressure Pain threshold3 weeksPressure algometry measured by digital algometer
Anxiety and Depression3 weeksHospital Anxiety and Depression Scale (HADS)
Muscular length3 weeksThe investigators measure the muscular length with an inclinometer

Countries

Spain

Outcome results

None listed

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