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investigating the effect of perturbation exercises and dry needling on the improvement of ankle sprain

investigating and comparison of the effect of perturbation exercises and dry needling technique on the improvement of chronic ankle sprain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190909044734N1
Enrollment
24
Registered
2020-02-06
Start date
2019-06-05
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Chronic ankle instability. M25.373

Interventions

Intervention 1: Intervention group: dry needle group with perturbation exercises. In this group, the muscles of the proneus longus and brevis and gastrocnemius and anterior tibialis were examined for

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Pain above 3 in numeric pain rate scale (NPRS) The instability score 25 or less in comberland ankle instability questionnaire Presence of trigger point in at least one of the muscles proneus longus, proneus brevis, gastrocnemius and anterior tibialis The absence of mechanical instability in affected ankle The experience of inversional instability in one ankle joint during previous six months

Exclusion criteria

Exclusion criteria: Lower limb or spinal column injury Neurologic or neuromuscular disease Vestibular system disorder Low back pain in previous six months Sensory changes in lower extremities History of lower limbs fractures, dislocation and biomechanical defects and any kind of orthopedic disorder Doing any rehabilitation and medical treatment for affected ankle during previous six months History of reumatological disease History of spinal column surgery Presence of spinal or lower limb deformity like bow leg, genu valgum or flat foot Consumption of sedative drug in previous week Vision problems those are not resolved with glasses For people who have banned dry needle technique such as weakened immune system vascular problems and abnormal bleeding Use of anticoagulants for injury and skin injuries Epilepsy Diabetes Pregnancy

Design outcomes

Primary

MeasureTime frame
Pain with NRS scale  and Performance with FAAM questionnaire. Timepoint: Before intervention, Immediately after completion of treatment, One month after intervention. Method of measurement: NPRS scale, FAAM questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Abbasi

Shiraz University of Medical Sciences

leabbasi@sums.ac.ir+98 71 3627 1551

Outcome results

None listed

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