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Comparison of Kinesio Taping and Dry Needling in Grade 1, 2 Knee Osteoarthritis

Comparison of Kinesio Taping and Dry Needling in the Management of Grade 1, 2 Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06086717
Enrollment
30
Registered
2023-10-17
Start date
2022-01-12
Completion date
2023-01-31
Last updated
2023-10-27

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

Conditions

Osteoarthritis, Knee

Keywords

Dry Needling, Joint Flexibility, Kinesio Tape, Knee Osteoarthritis, Pain, Quality of Life

Brief summary

This study's aim was: \- To determine the effects of kinesio taping and dry needling on pain, ROMs, functional mobility, and quality of life in knee OA patients.

Detailed description

This was a randomized clinical trial in which Grade 1, 2 Knee Osteoarthritis patients were randomized into two groups: Group-A and Group-B. Group-A participants received Kinesio taping while Group-B participants received dry needling as an adjunct to the conventional physical therapy treatment. The intervention was carried out for four weeks with frequency of two sessions per week. Outcome measures were assessed at baseline, after two weeks, and after 4 weeks, using Visual Analog Scale (VAS), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Knee Range of Motion (ROM), and SF-12 Quality of Life Questionnaire.

Interventions

OTHERKinesio Taping

One Y-shaped strap with 25% stretch was applied from the mid third of the thigh over the rectus femoris, then its ends directed toward the tibial tuberosity by enwrapping the patella from lateral and medial sides. In 45° knee flexion one eye strap from medial to lateral was applied through the collateral medial and lateral ligaments. For the facilitation of VMO 1 eye strap with 25% stretch from medial aspect of thigh to quadriceps tendon. Lastly, 1 eye strap with 25% stretch from tibial tuberosity to lateral aspect of thigh for inhibition of Vastus lateralis

OTHERDry Needling

Following a protocol according to patient and limb, the tensor fasciae latae, hip adductors, hamstrings, quadriceps, gastrocnemius, and popliteus muscles were properly examined in each subject. These muscles are frequently involved in muscle-related knee pain. Patients with knee OA who had at least one active MTrP that produced pain were recruited. Patients received a total of 8 DN sessions (2 sessions per week for 4 weeks) at all MTrPs of the lower limbs using the fast-in and fast-out technique (the needle was moved up and down within the muscle).

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Concurrent Parallel Randomized Clinical Trial

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Clinically diagnosed patients of grade 1, 2 knee OA (Kallgren and Lawrence). * Pain and/or tenderness around knee joint * Knee OA patients with tightness in Quadriceps, Hamstrings, and Iliotibial band. * Patients with pain of \>4 on VAS.

Exclusion criteria

* Patients who had received Intra-articular Steroid injections in knee joints. * Patients who had suffered a traumatic injury to knee joint within past 6 months prior to this study. * Patients with any surgical intervention to the knee joints. * Patients with peripheral vascular disease. * Patients with diagnosed tumors, malignancies, infection associated with knee joint. * Patients with lower limb metallic implants.

Design outcomes

Primary

MeasureTime frameDescription
Pain ScoreBaseline, after 2 weeks, and after 4 weeks.Pain was measured using Visual Analog Scale on a score from zero (0=no pain) to ten (10=worst pain possible).
Knee ROMBaseline, after 2 weeks, and after 4 weeks.Knee ROM (flexion and extension) was assessed using universal goniometer.

Secondary

MeasureTime frameDescription
WOMAC ScoreBaseline, after 2 weeks, and after 4 weeks.Patients' pain, stiffness, and physical functioning of the joints was assessed using WOMAC scale.
Quality of Life ScoreBaseline, after 2 weeks, and after 4 weeks.Patients health-related quality of life was assessed using SF-12 questionnaire.

Countries

Pakistan

Outcome results

None listed

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