the effect of physiotherapy on knee pain

the effect of treatment based on movement system impairment classification theory in people with knee pain (a randomized control trial)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190222042801N1

Enrollment

Registered

2020-12-17

Start date

2019-04-21

Completion date

Unknown

Last updated

2021-01-05

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

Conditions

knee pain. knee Pain

Interventions

Intervention 1: Intervention group 1: Patients with knee rotation syndrome with valgus who are given specific treatment based on movement system impairment classification theory within 10 sessions in

Routine physiotherapy treatments including: 1- Hot pack

Eligibility

Sex/Gender

All

Age

18 Years to 50 Years

Inclusion criteria

Inclusion criteria: patients with knee rotation syndrome or pateller lateral glide syndrome knee pain during running or jumping knee pain at least 3 on visual analog scale

Exclusion criteria

Exclusion criteria: Pregnancy

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week the end of follow up period. Method of measurement: with visual analog scale.;Disability level. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week the end of follow up period. Method of measurement: with knee injury and osteoarthritis outcome score questionnaire.;Function level. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week, the end of follow up period. Method of measurement: with lower extremity functional scale questionnaire.;Knee joint frontal plane projection angle. Timepoint: Before treatment beginning, at the end of the sixth week after treatment finishing and the end of the twelfth week, after follow up period. Method of measurement: with video camera and Kinovea software.	—

Measure

Time frame

Pain intensity. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week the end of follow up period. Method of measurement: with visual analog scale.;Disability level. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week the end of follow up period. Method of measurement: with knee injury and osteoarthritis outcome score questionnaire.;Function level. Timepoint: Before treatment beginning, at the end of the third week in the middle of treatment period, at the end of the sixth week after treatment finishing and at the twelfth week, the end of follow up period. Method of measurement: with lower extremity functional scale questionnaire.;Knee joint frontal plane projection angle. Timepoint: Before treatment beginning, at the end of the sixth week after treatment finishing and the end of the twelfth week, after follow up period. Method of measurement: with video camera and Kinovea software.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammad Jafar Shaterzadeh

Ahvaz University of Medical Sciences

Shaterzadeh.pt@gmail.com+98 33743103

Outcome results

None listed

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