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Immediate Effect of Pain relief by Ultrasound in Individual with Sub-Acute Ankle Sprain: A Randomized Controlled Trial

Immediate Effect of Pain relief by Ultrasound in Individual with Sub-Acute Ankle Sprain: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200423002
Enrollment
Unknown
Registered
2020-04-23
Start date
2020-04-24
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Ankle Sprain Ankle sprain, Sub-Acute phase, Lateral ankle sprain

Interventions

In the treatment group, participants received US according to thermal effect . US treatment intensity was set at 0.25 W/cm2 with a duty cycle of 100% and frequency of 3 MHz. A circular stroke techniqu
Experimental Device,Sham Comparator Device

Sponsors

THE 90TH Anniversary of Chulalongkorn University Scholarship (waiting for application)
Lead Sponsor
Medical Division of Armed Forces Academies Preparatory School
Collaborator

Eligibility

Sex/Gender
All
Age
16 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1)Males or females aged 16-55 years 2)Diagnosed by a physician with lateral ankle sprain (Grade I-II) at least 4 days and up to 14 days with visual analog scale at least 30/100 3)Adequate ability to communicate in Thai and to cope with a visual analog scale for pain

Exclusion criteria

Exclusion criteria: 1)Have redness and warmth at area of ankle sprain 2)Received radiotherapy in the last 6 months 3)Have numbness of lower extremity 4)Have vestibular problems confirmed by medical history 5)Have contraindications of US

Design outcomes

Primary

MeasureTime frame
Pain intensity Before and after intervention Visual analog scales was used to assess pain intensity during rest (VAS-R) and on weight-bearing

Secondary

MeasureTime frame
Range of motion Before and after intervention Range of motion (ROM) of ankle and subtalar joint were measured by a digital goniometer in dorsiflexion and plantarflexion,Plantar pressure Before and after intervention Plantar pressure , contact area, and center of pressure were measured by baropodometer.

Countries

Thailand

Contacts

Public ContactLt.Thongchai Suksri

Chulalongkorn University

sakeereenlove@gmail.com0895396479

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026