The effects of treadmill walking in low back pain

Pilot study:the effects of 10%uphill treadmille walking in comparison to level treadmill walking in patients with nonspescific chronic low back pain.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016090321479N3

Enrollment

Registered

2016-09-12

Start date

2016-07-05

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

low back pain. Dorsalgia, unspecified

Interventions

Intervention 1: Intervention:four weeks intervention,three sessions every week.include:electrotherapy,mobilisation and treadmill walking on 10%uphill inclination. Intervention 2: Control group :four

Rehabilitation

Intervention:four weeks intervention,three sessions every week.include:electrotherapy,mobilisation and treadmill walking on 10%uphill inclination.

Control group :four weeks intervention,three sessions every week.include:electrotherapy,mobilisation and treadmill walking on level surface.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria:men and women,chronic nonspescific low back pain. Exclusion criteria:previous history spinal canal surgery; BMI>30; previous history of back fracture or instability; previous history of chronic heart failure or coronary disease; fracture or sever degenerative changes in lower limb joints; lower limb arthroplasty; pregnant women; knee pain; scoliosis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Back endurance test. Timepoint: Before 1th session,12th session,two m1.before the study at first session,2.fourth week(.12th session),3.two month after the final sessioonth afther the final session. Method of measurement: Modified sorenson test.	—

Secondary

Measure	Time frame
Disability. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.;Fear avoidance belief. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.;Vas. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.	—

Measure

Time frame

Disability. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.;Fear avoidance belief. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.;Vas. Timepoint: 1.before the study at first session,2.fourth week(.12th session),3.two month after the final session. Method of measurement: Questionnaire.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Abdolkarim Karimi

Esfahan University of Medical Sciences

a_karimi@rehab.mui.ac.ir+98 31 3668 1853

Outcome results

None listed

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