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Dry Needling and Kinesio Taping as Adjuncts to Strength Training on Pain, Functional Mobility, and Quality of Life in Patients With Knee Osteoarthritis

Comparative Effects of Dry Needling and Kinesio Taping as Adjuncts to Strength Training on Pain, Functional Mobility, and Quality of Life in Patients With Knee Osteoarthritis: A Three-Arm Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07710235
Enrollment
50
Registered
2026-07-17
Start date
2024-11-01
Completion date
2025-12-01
Last updated
2026-07-17

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

Conditions

Knee Osteoarthritis (OA)

Keywords

Knee osteoarthritis; Dry needling; Kinesio taping; Strength training; Quality of life

Brief summary

To compare the effects of dry needling and Kinesio taping, each combined with strength training, on pain, functional mobility, and quality of life in patients with knee OA.

Detailed description

Background: Knee osteoarthritis (OA) is a progressive degenerative joint condition characterized by pain, myofascial trigger points, muscular weakness, and impaired functional mobility, ultimately affecting quality of life. Strength training is widely recommended as a first-line conservative treatment; however, residual pain and myofascial dysfunction may limit optimal recovery. Dry needling has been shown to deactivate trigger points and reduce local muscle hypertonicity, while Kinesio taping is proposed to modulate pain and support proprioception and muscle function through cutaneous and fascial mechanisms. Comparative evidence on the added benefit of these two adjunct techniques alongside strength training in knee OA remains scarce. Objective: To compare the effects of dry needling and Kinesio taping, each combined with strength training, on pain, functional mobility, and quality of life in patients with knee OA. Methodology: A three-arm parallel-group randomized controlled trial was conducted on 50 participants diagnosed with knee OA (Kellgren-Lawrence grade II-III), randomly allocated into three groups using a computer-generated random sequence with allocation concealment. Group A received dry needling combined with strength training, Group B received Kinesio taping combined with strength training, and Group C received strength training alone as the control group. Interventions were administered three times per week for 6 weeks. Outcome measures included the Numeric Pain Rating Scale (NPRS) for pain, the Timed Up and Go (TUG) test for functional mobility, and the WHOQOL-BREF for quality of life, assessed at baseline and post-intervention (6 weeks). Data were analyzed using repeated-measures ANOVA and post-hoc comparisons, with significance set at p\<0.05.

Interventions

BEHAVIORALDry Needling Combined with Strength Training

Dry Needling Combined with Strength Training were administered three times per week for 6 weeks

BEHAVIORALKinesio Taping Combined with Strength Training

Kinesio Taping Combined with Strength Training were administered three times per week for 6 weeks

BEHAVIORALStrength Training

Strength Training were administered three times per week for 6 weeks

Sponsors

Foundation of Medical Research and Laboratories, Pakistan
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
45 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Patient with knee osteoarthritis, Age between 45-65 years, VAS 7 or above. \-

Exclusion criteria

Known allergic conditions, refused to give written consent to participate in the study not fallen in inclusion criteria. \-

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)6 weeksThe value were taken at base line and after 6 weeks of intervention
Timed Up and Go (TUG)6 weeksThe value were taken at base line and after 6 weeks of intervention
WHOQOL-BREF6 weeksThe value were taken at base line and after 6 weeks of intervention

Countries

Pakistan

Contacts

STUDY_DIRECTORMalika Hassan

fmr.labs@medicalresearchforum.net

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 18, 2026