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Acute Effect of Isometric Excercise on Pain Sensitivity in Adults With Chronic Low Back Pain

T

Taif University

Status

Enrolling

Conditions

Chronic Low Back Pain (CLBP)

Treatments

Other: Multiple Isometric wall squat exercise + Double Leg Lower with Isometric Hold
Other: Multiple repetition isometric wall squat
Other: Control quiet seated rest

Study type

Interventional

Funder types

Other

Identifiers

NCT06963658
ISO-Ex 0011112222

Details and patient eligibility

About

Randomized control trial to examine the immediate effect of isometric exercise on pressure pain threshold (PPT) in adults with chronic low back pain. The secondary aim of this study was to investigate the acute effects of isometric exercise on clinical pain intensity.

Full description

Participants will attend a single visit to the hospital for two hours, which will include collecting demographic details and clinical characteristics through self-reported assessment scales. After that, outcome measures (pain sensitivity and current low back pain intensity) were collected prior to the intervention and repeated immediately post-intervention.

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

  1. participants aged ≥18 years or older
  2. participant diagnosed with non-specific chronic lower back pain (> 12 weeks)
  3. Able to perform physical therapy excercise . Exclusion criteria : The study will exclude

1- pregnant women 2- lactating women for one or less than one year post-natal. 3- any certain medical conditions that could interfere with physical activity, including:

  • uncontrolled diabetes
  • cardiovascular problem
  • orthopedic impairments
  • balance problems. 4-serious spinal pathologies :
  • infection
  • fractures
  • tumors
  • inflammatory diseases like ankylosing spondylitis 5- neurological compromise,
  • spinal nerve compromise
  • cauda equina syndrome

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

90 participants in 3 patient groups

Multiple repetition isometric wall squat
Experimental group
Description:
Participants were directed to rest their backs against the wall with shoulder width apart and feet parallel, then descend until they achieve an angle of 100 degrees at knee joint. The knee joint angle was assessed using a goniometer placed on the lateral epicondyle of the knee, aligned with the femur, while the anchor arm was aligned with the lateral malleolus. They were instructed to maintain the isometric hold for up to three minutes, or until volitional fatigue was reached.with a 30-second rest period between each squat hold.
Treatment:
Other: Multiple repetition isometric wall squat
Multiple Isometric wall squat exercise + Double Leg Lower with Isometric Hold
Experimental group
Description:
Participants were directed to rest their backs against the wall with shoulder width apart and feet parallel, then descend until they achieve an angle of 100 degrees at knee joint. The knee joint angle was assessed using a goniometer placed on the lateral epicondyle of the knee, aligned with the femur, while the anchor arm was aligned with the lateral malleolus. They were instructed to maintain the isometric hold for up to three minutes, or until volitional fatigue was reached.with a 30-second rest period between each squat hold. Immediately post 60 second rest, Determine the participant's maximum angle using the double leg lowering test from supine position let the participant with both legs straightened before lifting the posterior hip, lowering the legs to a specific angle. Turn on the stopwatch. Hold the position near--maximally, try to achieve on (IES=9/10) and hold for the longest duration. They should reach 4 minutes for 3 repetition with 30 seconds rest between repetition
Treatment:
Other: Multiple Isometric wall squat exercise + Double Leg Lower with Isometric Hold
Control quiet seated rest
Experimental group
Description:
The CON group served as the control group and did not perform any exercise. Participants were instructed to sit quietly in a standard height stationary clinical room patient chair for the entire eight minutes.
Treatment:
Other: Control quiet seated rest

Trial contacts and locations

1

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Central trial contact

Hosam A Alzahrani, PHD; Asma A Alqahtani, B.S.C

Data sourced from clinicaltrials.gov

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