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Clinical Trials/CTRI/2023/01/048829
CTRI/2023/01/048829Not yet recruitingPhase 2/3

Effectiveness of Tendon Neuroplastic Training and Oxygen Therapy in athletes with patellar tendinopathy

Kunal Bijalwan1 site in 1 country68 target enrollmentStarted: October 1, 2023Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
68
Locations
1
Primary Endpoint
Victorian Institute of sports medicine (VISA-P)

Study Overview

Brief Summary

Patellar Tendinopathy is one of the major lower limb tendinopathies affecting athletes, major factors that affect the athlete in patellar tendinopathy are pain, tenderness, reduced ability to transfer loads, and overall poor performance on and off the field. Recent studies on tendon neuroplastic training and oxygen therapy show a positive effect on the condition, but there is very less data that combines these two different entities in patellar tendinopathy.

The objectives of this study are to:-

  1. To test the efficacy of tendon neuroplastic training and oxygen therapy combined on pain levels in athletes with patellar tendinopathy.

  2. To test the efficacy of tendon neuroplastic training and oxygen therapy combined on tenderness levels in athletes with patellar tendinopathy.

  3. To test the efficacy of tendon neuroplastic training and oxygen therapy combined on the quality of life of an athlete

  4. To test the efficacy of these interventions alone in athletes with patellar tendinopathy.

  5. To compare the effectiveness of tendon neuroplastic training combined with oxygen therapy with a controlled group consisting of standard rehabilitation for patellar tendinopathy.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Participant Blinded

Eligibility Criteria

Ages
15.00 Year(s) to 35.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Athletes, Anterior Knee pain, Patellar tendinopathy, Age group 15-35 years, inferior pole of patella tenderness, Positive single leg declined squat test.

Exclusion Criteria

  • Any Musculoskeletal pathology affecting their lower leg in the last six months, History of knee surgery, on medication, any respiratory condition, already enrolled in a physiotherapy rehabilitation program.

Outcomes

Primary Outcomes

Victorian Institute of sports medicine (VISA-P)

Time Frame: All the above parameter will be taken at baseline 0 weeks, the next recording will be at the end of 2 week and last recording will be at the end 4 weeks

Tenderness– Algometer

Time Frame: All the above parameter will be taken at baseline 0 weeks, the next recording will be at the end of 2 week and last recording will be at the end 4 weeks

Pain–Numeric Pain Rating Scale (NPRS)

Time Frame: All the above parameter will be taken at baseline 0 weeks, the next recording will be at the end of 2 week and last recording will be at the end 4 weeks

Secondary Outcomes

  • Quality of life– WHOQOL-100(This parameter will be taken at baseline 0 weeks, then at the end of 2 weeks and the last recording will be taken at the end of 4 week)

Investigators

Sponsor
Kunal Bijalwan
Sponsor Class
Other [self]

Study Sites (1)

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