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Effect of kinesiotaping on postural control in subjects with ACL deficiency: a randomized clinical trial

Effect of kinesiotaping on postural control in subjects with ACL deficiency: a randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016122131506N1
Enrollment
36
Registered
2017-06-08
Start date
2017-05-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Anterior Cruciate Ligament Tear. Sprain and strain involving (anterior)(posterior) cruciate ligament of knee

Interventions

Intervention 1: Intervention group: A 5-cm-wide Kinesiotape (Ares, Korea) will be used in treatments. Few hours after shaving the area of the skin to be taped, Y-shaped tapes will be applied in origi
Rehabilitation
Intervention group: A 5-cm-wide Kinesiotape (Ares, Korea) will be used in treatments. Few hours after shaving the area of the skin to be taped, Y-shaped tapes will be applied in origin-insertion dire
Control group: Placebo kinesiotape will be applied without tension on the front and back side of the knee.

Sponsors

Vice chancellor for research, Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Participants must be between ages 18-35? complete and non- complete tear of anterior cruciate ligament with and without meniscal injury. Exclusion criteria: ACLD (ACL deficient) subjects will be excluded if they had any serious neurological disorders? musculoskeletal disorders (except for ACLD)? history of falling? narcotic usage 48 hours before test? usage of alcohol 48 hours before test.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postural Sway. Timepoint: Before intervention, Immediately after internention. Method of measurement: Force Platform Device.

Secondary

MeasureTime frame
Disability. Timepoint: Before and two days after intervention. Method of measurement: Koos Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Salman Nazary-Moghadam

Mashhad University of Medical Sciences

nazary_salman@yahoo.com00

Outcome results

None listed

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