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ChondromalaciaNCT06561568

Additional Effects of Kinesio Taping on Knee Joint Proprioception and Spatiotemporal Gait Parameters in Patient With Chrondromalacia Patellae

A study testing Conventional physical therapy and Kinesiotaping in people with Chondromalacia, run by Foundation University Islamabad at 1 site in Pakistan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 15 to 60 years
Conditions the study is for
Chondromalacia
What is being tested?
Conventional physical therapy and Kinesiotaping
Could I receive a placebo?
No, everyone receives an active treatment
How many people
46 participants
Where
1 sitePakistan
Study dates
10 Jun 2024to 30 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 60 years
  • All sexes
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • 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
Show all 9Show fewer
  • Patellar instability
  • Previous surgery of lower limb
  • Positive findings on examination of knee ligaments, menisci and bursa.

Who cannot join

  • -

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Foundation University College of Physical Therapy

    Rawalpindi, 46000

Other trials in Pakistan

About this study

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.

Conditions
Chondromalacia
Being tested
Conventional physical therapy, Kinesiotaping
Medical subject headings
Cartilage Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Conventional physical therapyDiagnostic test

    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.

  • KinesiotapingOther

    Kinesio tape will be applied on Vastus medialis Oblique and around the patella.

    • Frequency: 3 times a week for 4 weeks.
Study groups in NCT06561568
Study groupRoleWhat they receive
Conventional physical therapy (exercise therapy) groupActive comparatorGroup 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.
Receives: Diagnostic Test: Conventional physical therapy
Kinesio taping + Conventional physical therapy groupExperimentalGroup 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.
Receives: Diagnostic Test: Conventional physical therapy; Other: Kinesiotaping

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proprioception

    Proprioception will be measured using goniometer.

    Measured: 4 weeks

  2. 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.

    Measured: 4 weeks

  3. 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.

    Measured: 4 weeks

  4. Gait Speed

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

    Measured: 4 Weeks

  5. 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)

    Measured: 4 Weeks

  6. 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

    Measured: 4 weeks

  7. 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)

    Measured: 4 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Aug 2024
  2. Study start10 Jun 2024
  3. Primary completion10 Dec 2024 (estimated)
  4. Study completion30 Dec 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
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.
Masking
None (open label)
Enrolment
46 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06561568
Sponsor's protocol ID
FUI/CTR/2024/20
Status last verified
Jul 2024
First submitted
30 Jul 2024
Last updated
20 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Conventional physical therapy and Kinesiotaping in people with Chondromalacia, run by Foundation University Islamabad at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 20 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proprioception (time frame: 4 weeks). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2024.

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