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Comparison of the effect of high level laser therapy and exercise-based rehabilitation in patients with ankle sprain

Comparison of the effect of high level laser therapy and exercise-based rehabilitation on pain severity and ankle instability in patients with ankle sprain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241215064061N1
Enrollment
20
Registered
2025-02-03
Start date
2024-12-09
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Ankle sprain. Sprain and strain of ankle

Interventions

Intervention 1: First intervention group: High-power laser therapy: This group will undergo intervention using a high-power

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: • Age 18 to 65 years • Confirmed diagnosis of ankle sprain with grade 1 and 2 • Occurrence of ankle sprain at any time while undergoing treatment with cast or splint or conservative treatment and are now referred to this clinic. • Patient consent to enter the study

Exclusion criteria

Exclusion criteria: No history of previous ankle fracture, previous ankle surgery, and concurrent musculoskeletal injuries of other organs, No history of receiving treatments other than the study treatment, No history of other rheumatological diseases involving the musculoskeletal system, such as rheumatoid arthritis or systemic lupus erythematosus, No history of rehabilitation from other centers or no skin wound at the site of the sprain, No history of ankle fracture, No history of ankle surgery, Incomplete patient file information

Design outcomes

Primary

MeasureTime frame
Pain intensity based on visual analog scale (VAS). Timepoint: The VAS number to measure pain intensity was measured before the intervention, 2 weeks after the intervention, and after its completion (one month) in both the high-power laser therapy and exercise-based rehabilitation groups. Method of measurement: VAS Scoring System: Patients' pain scores are measured using a Visual Analogue Scale (VAS). This scale is usually designed as a straight line 10 cm long, with the words "no pain" written on one side and "worst possible pain" on the other, and each point on the line represents a level of pain intensity from 0 to 10.;Ankle instability. Timepoint: The BESS score to measure ankle instability was recorded before the intervention, 2 weeks after the intervention, and after its completion (one month) in both the laser therapy and rehabilitation groups. Method of measurement: Balance Error Scoring Test (BESS): This test is a quantitative test that counts and scores defined errors during the test. In a single-leg stance, the subject stands on the injured side, flexing the opposite knee 40 to 50 degrees and the opposite hip 20 to 30 degrees. During the test, if the subject cannot maintain balance for at least 5 seconds, the test is considered incomplete. The maximum standard error score for each test session is 10.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hossein Bagheri

Mazandaran University of Medical Sciences

mhb.9195@gmail.com+98 11 3336 6552

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026