Efficacy of Tecar Device With Exercises in Ankle Sprain

NCT ID: NCT06934629

Last Updated: 2025-04-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-15

Study Completion Date

2025-06-30

Brief Summary

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The goal of this clinical trial is to evaluate the effect of applying TECAR therapy during active therapeutic exercises on pain, ankle dynamic balance, proprioception, and daily function in patients with acute ankle sprain.

the main questions it aims to answer are:

* Does there is a significant effect of applying TECAR therapy during active exercise after acute lateral ankle sprain on Pain?
* Does there is a significant effect of applying TECAR therapy during active exercise after acute lateral ankle sprain on balance?
* Does there is a significant effect of applying TECAR therapy during active exercise after acute lateral ankle sprain on proprioception?
* Does there is a significant effect of applying TECAR therapy during active exercise after acute lateral ankle sprain on daily function? The patients will be randomly divided into two groups. The control group (A) will receive the conventional therapy which is ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training. The experiment group (B) will receive conventional therapy with TECAR therapy application during active therapeutic exercises.

Treatment will be for 4 weeks with 2 sessions per week. TECAR application will be 20 mins per session (10 mins capacitive and 10 mins resistive).

To the best of the researchers' knowledge, no study has proved the effects of applying TECAR therapy during active therapeutic exercises after an acute lateral ankle sprain has yet been done. Thus, the purpose of the present study was to prove if there an effect of applying TECAR therapy during active therapeutic exercises included in the conventional physiotherapy (PRICE with therapeutic exercises) and conventional physiotherapy alone on pain, ankle dynamic balance, proprioception, and daily function in subjects with an acute lateral ankle sprain.

Detailed Description

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Conditions

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Ankle Sprain TECAR Therapy TECAR Therapy Efficacy in the Treatment of Ankle Sprain Ankle Dynamic Balance Ankle Pain Ankle Proprioception

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

FACTORIAL

Treatment will be for 4 weeks with 2 sessions per week. TECAR application will be 20 mins per session (10 mins capacitive and 10 mins resistive) during ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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TECAR therapy group

traditional therapeutic exercises for ankle sprain and TECAR therapy application during exercises .

Group Type EXPERIMENTAL

TECAR therapy

Intervention Type DEVICE

TECAR application will be 20 mins per session (10 mins capacitive and 10 mins resistive) during ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training.

Conventional therapy group

traditional therapeutic exercises for ankle sprain

Group Type ACTIVE_COMPARATOR

therapeutic exercises

Intervention Type OTHER

the conventional therapy which is ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training.

Interventions

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TECAR therapy

TECAR application will be 20 mins per session (10 mins capacitive and 10 mins resistive) during ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training.

Intervention Type DEVICE

therapeutic exercises

the conventional therapy which is ankle and subtalar ROM in a pain-free range, calf muscle stretch, ankle strengthening exercises against resistance bands in all directions, weight-bearing exercise, forward lunges, bilateral and unilateral squats, bilateral and unilateral heel raises against bodyweight resistance, and balance training.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Gender will be male and female.
* Age from 20-40 years old.
* Grade \| and \|\| lateral ankle sprain.
* Patients who will be diagnosed and referred by orthopedic surgeon.
* acute stage of lateral ankle sprain.
* BMI ≤ 30.
* Positive confirming tests.

Exclusion Criteria

* Ankle fractures such as talus bone fracture, tibia fracture, ankle dislocation.
* Unwilling to continue treatment.
* Contraindications to use TECAR therapy, such as pregnancy, the presence of malignant tissue, tumors, in the ankle, and electrical devices implanted in the body.
* Grade \|\|\| ankle sprain.
* Systematic diseases such as rheumatoid arthritis.
* Recently received intra-steroid injection
* Pain exacerbation during the intervention.
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Asmaa Morsy Elsayed Ali Morsy

resident physiotherapist registered for master degree

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Andalusia hospital in Alexandria

Alexandria, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Asmaa M Elsayed, student of master's degree

Role: CONTACT

+201066744799

Facility Contacts

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Asmaa Morsy

Role: primary

01066744799

Other Identifiers

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P.T.REC/012/005596

Identifier Type: -

Identifier Source: org_study_id

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