NCT06561568

Brief Summary

Chondromalacia patellae (CMP), also known as runner's knee, is characterized by anterior knee pain (AKP) and typically occurs in youngsters. Causes of chondromalacia patellae include micro trauma wear and tear, post traumatic injuries and muscular imbalance. In Chondromalacia patella pain is behind or around the patella caused by stress in the patellofemoral joint that usually provoked by climbing stairs, squatting, and sitting with flexed knees for longer time periods. Patients of CMP presents with patellar mal-tracking, muscular weakness, proprioceptive deficit. Exercise training has been proven beneficial for CMP patients but additive effect of kinesio taping along with exercise have not been seen yet in these patients. The study will help people with chondromalacia patellae to improve their quality of life. The findings will contribute to future research in chondromalacia patellae management.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
46

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 10, 2024

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

July 30, 2024

Completed
21 days until next milestone

First Posted

Study publicly available on registry

August 20, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 10, 2024

Completed
20 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2024

Completed
Last Updated

August 20, 2024

Status Verified

July 1, 2024

Enrollment Period

6 months

First QC Date

July 30, 2024

Last Update Submit

August 19, 2024

Conditions

Outcome Measures

Primary Outcomes (7)

  • Proprioception

    Proprioception will be measured using goniometer.

    4 weeks

  • Pain intensity

    Pain will be measured using numeric pain rating scale (NPRS) It is a self-rated scale where patient rate their pain from 0-10. 0 shows no pain where 10 shows worst pain.

    4 weeks

  • Functional status

    Functional status is assessed by lower extremity functional scale LEFS. The LEFS is scored on a scale of 0 to 80, with higher scores indicating better lower limb function. The interpretation of the scores is based on following categories. 0-20 Severe Functional limitation.21-40 moderate functional limitation and 41 and above is good functional status.

    4 weeks

  • Gait Speed

    Gait analysis will be done to analyze speed.. A greater speed signifies positive outcome and prognosis. Speed = distance(m) x time(s)

    4 Weeks

  • Gait cadence

    Gait analysis will be done to analyze cadence. A greater cadence signifies positive outcome and prognosis. Cadence(steps/min) = steps countedx60/ time(s)

    4 Weeks

  • Gait cycle time

    Gait analysis will be done to analyze cycle time. A greater cycle time signifies positive outcome and prognosis. Cycle time(s)=time(s) x2/steps counted

    4 weeks

  • Stride length

    Gait analysis will be done to analyze stride length. A greater stride length signifies positive outcome and prognosis. Stride Length(m)=Speed(m/s)xcycle time(s)

    4 weeks

Study Arms (2)

Conventional physical therapy (exercise therapy) group

ACTIVE COMPARATOR

Group A will receive this conventional physical therapy protocol for chondromalacia patellae * they will perform stretches to warm up and cool down. Resistance training ,in which patient will perform each exercise for 3 sets of 10 repetitions. Each repetition will be given with a 10 second hold. * Frequency: 3 times a week for 4 weeks.

Diagnostic Test: Conventional physical therapy

Kinesio taping + Conventional physical therapy group

EXPERIMENTAL

Group B will be given kinesio taping with conventional physical therapy protocol for chondromalacia patellae. .Kinesio tape will be applied on Vastus medialis Oblique and around the patella. • Frequency: 3 times a week for 4 weeks. They will perform stretches to warm up and cool down. Resistance training ,in which patient will perform each exercise for 3 sets of 10 repetitions. Each repetition will be given with a 10 second hold. Frequency: 3 times a week for 4 weeks.

Diagnostic Test: Conventional physical therapyOther: Kinesiotaping

Interventions

Conventional physical therapy protocol for chondromalacia patellae consist of stretches to warm up and cool down Resistance training ,in which patient will perform each exercise for 3 sets of 10 repetitions. Each repetition will be given with a 10 second hold.

Conventional physical therapy (exercise therapy) groupKinesio taping + Conventional physical therapy group

Kinesio tape will be applied on Vastus medialis Oblique and around the patella. • Frequency: 3 times a week for 4 weeks.

Kinesio taping + Conventional physical therapy group

Eligibility Criteria

Age15 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Both genders
  • Age: Under 60yrs
  • Pain while stair climbing, kneeling, squatting, changing position from sitting to standing and running
  • Exclusive criteria:
  • Instability of tibiofemoral joint
  • Subluxation of patellofemoral joint
  • Patellar instability
  • Previous surgery of lower limb
  • Positive findings on examination of knee ligaments, menisci and bursa.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Foundation University College of Physical Therapy

Rawalpindi, 46000, Pakistan

Location

MeSH Terms

Conditions

Cartilage Diseases

Condition Hierarchy (Ancestors)

Musculoskeletal DiseasesConnective Tissue DiseasesSkin and Connective Tissue Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This is a randomized controlled trial having two groups. KInesio taping along with conventional physical therapy will be applied in one group and the second will receive conventional physical therapy only. Both groups will be recruited concurrently.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 30, 2024

First Posted

August 20, 2024

Study Start

June 10, 2024

Primary Completion

December 10, 2024

Study Completion

December 30, 2024

Last Updated

August 20, 2024

Record last verified: 2024-07

Locations