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Functional Hip Strength Improvement in Knee Osteoarthritis Following Single-Dose PRP and a 6-Week Home Exercise Program

F

Firat University

Status

Completed

Conditions

Knee Osteoarthritis (OA)

Treatments

Biological: Platelet-Rich Plasma (PRP) Injection
Behavioral: Home Exercise Program

Study type

Interventional

Funder types

Other

Identifiers

NCT07307118
FU_MGBeydagi_PRP_B_2025/12/150

Details and patient eligibility

About

This single-group longitudinal study evaluated changes in hip stability isometric strength, knee muscle strength, and activity-related pain in women with knee osteoarthritis following a single-dose intra-articular platelet-rich plasma (PRP) injection and a 6-week home exercise program. Outcomes were assessed at baseline (5 days post-injection), week 6, and week 12. The intervention included strengthening exercises for knee and hip muscle groups performed three times per week and regular walking encouragement with weekly phone follow-up for adherence.

Full description

Participants with unilateral symptomatic knee osteoarthritis performed a standardized 6-week home strengthening program (knee extensors/flexors; hip extensors/abductors/external rotators) three times weekly and were encouraged to walk regularly. Hip Stability Isometric Test (HipSIT), quadriceps/hamstring strength (hand-held dynamometry, normalized to body mass), and activity pain (VAS 0-10) were measured at baseline, week 6, and week 12 to evaluate functional strength and symptom changes after PRP plus exercise.

Enrollment

27 patients

Sex

Female

Ages

45 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female patients aged 45-70 years.
  • Radiographic knee osteoarthritis: Kellgren-Lawrence grade II-III in the affected knee and grade II or less in the unaffected knee.
  • Unilateral knee pain during activity with VAS score ≥5 (for at least the past 3 months).
  • Referred to physiotherapy following a unilateral single-dose PRP injection.

Exclusion criteria

  • Any intra-articular knee injection within the past 6 months.
  • Regular lower-extremity strengthening exercise or non-pharmacological treatment for knee OA within the past 6 weeks.
  • History of lower-extremity surgery.
  • History of neurological, rheumatological and/or cognitive diseases.
  • Unable to use a telephone.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

27 participants in 1 patient group

Single Group: PRP Injection + Home Exercise Program
Experimental group
Description:
All participants received a unilateral single-dose intra-articular platelet-rich plasma (PRP) injection for symptomatic knee osteoarthritis, followed by a 6-week home-based strengthening and functional exercise program performed 3 times per week. The exercise program targeted knee extensors/flexors and hip extensors/abductors/external rotators. Participants were encouraged to walk at least 30 minutes on at least 5 days per week and were contacted weekly by phone to support adherence.
Treatment:
Behavioral: Home Exercise Program
Biological: Platelet-Rich Plasma (PRP) Injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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