NCT05288946

Brief Summary

The purpose of this study is to investigate the effect of segmental control exercises program on hamstring peak torque, pain, function, and ROM in patients with non-specific low back pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 11, 2022

Completed
10 days until next milestone

First Posted

Study publicly available on registry

March 21, 2022

Completed
7 days until next milestone

Study Start

First participant enrolled

March 28, 2022

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 15, 2022

Completed
Last Updated

October 31, 2022

Status Verified

October 1, 2022

Enrollment Period

2 months

First QC Date

March 11, 2022

Last Update Submit

October 27, 2022

Conditions

Keywords

segmental stabilization exerciselow back painpeak torque

Outcome Measures

Primary Outcomes (1)

  • peak torque

    isokinetic will be used for measuring hamstring peak torque

    up to four weeks

Secondary Outcomes (2)

  • pain intensity

    up to four weeks

  • disability

    up to four weeks

Study Arms (3)

local segmental control and closed kinetic chain

EXPERIMENTAL

the patients will receive local segmental control and closed kinetic chain three times a week for four weeks

Other: local segmental control and closed kinetic chainOther: traditional therapy

local segmental control and open kinetic chain

EXPERIMENTAL

the patients will receive local segmental control and open kinetic chain three times a week for four weeks

Other: local segmental control and open kinetic chainOther: traditional therapy

traditional therapy

ACTIVE COMPARATOR

the patients will receive traditional therapy three times a week for four week

Other: traditional therapy

Interventions

the patients will receive Lumbar multifidus activation and Transversus abdominis activation then closed kinetic chain exercise in the form of Stand-up position on unstable surface, Closed chain lunge exercises, with the addition of hand weights, Bridge in prone position, Bridge in supine position, Lateral Bridge

local segmental control and closed kinetic chain

the patients will receive Lumbar multifidus activation and Transversus abdominis activation then open kinetic chain in the form of Lower limb abduction, Knee extension in a supine position on a roller, Open chain exercise of the upper limb after co-contraction of transversus abdominis and multifidus.

local segmental control and open kinetic chain

the patients will receive exercise in the form of Sitting knee raise on gym ball to maintain stability in the presence of hip movement on a reduced base of support, abdominal slide to control action of the rectus abdominis while moving, Lying trunk curl with leg lift to strengthen upper and lower abdominals (figure 1-6), Basic superman to strengthen the spinal and hip extensors

local segmental control and closed kinetic chainlocal segmental control and open kinetic chaintraditional therapy

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • The patients had NS LBP Patients with age from 20 to 40 years for both genders.
  • The lumbar region of back pain lasts for 4 weeks \& more has not been diagnose as a specific disease or spinal abnormality.
  • Mild to moderate disability according to the Oswestry Disability Index (ODI) (up to 40%).
  • Shortening of hamstring.
  • The study populations must be willing to participate in the study.

You may not qualify if:

  • Neurological, systemic illness and infectious diseases such as rheumatologic diseases, tumor, cardiovascular disease.
  • Psychiatric/mental deficit
  • Patients who had a previous surgical history (within 6 months) were also excluded prior to the baseline assessment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cairo University

Giza, 11251, Egypt

Location

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
random generator
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: segmental stabilization exercises
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
principle investigator

Study Record Dates

First Submitted

March 11, 2022

First Posted

March 21, 2022

Study Start

March 28, 2022

Primary Completion

May 15, 2022

Study Completion

May 15, 2022

Last Updated

October 31, 2022

Record last verified: 2022-10

Locations