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Low Back PainSCSCRLCSNCT05505851

Sequential Core Stability Corrective Exercise Approach in Lower Crossed Syndrome

A study testing Sequential Core Stability Corrective Exercise Approach in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of the study will be to determine the effects of Sequential Core Stability Corrective Exercise Approach for Alignment and Muscle Function in Lower Crossed Syndrome. Read more about this study

Who is it for?
Ages 18 to 28 yearsHealthy volunteers can take part
Conditions the study is for
Low Back Pain
What is being tested?
Sequential Core Stability Corrective Exercise Approach
Could I receive a placebo?
No, everyone receives an active treatment
How many people
40 participants
Where
1 sitePakistan
Study dates
10 Feb 2024to 1 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 28 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • • Age group between 18 to 28 years
  • No current incidence of low back pain or past history of low back dysfunction
  • Kendall double leg lowering test: Abdominal muscle weakness to the extent of not being able to maintain posterior pelvic tilt during a double leg lowering test in supine position.
  • Diagnosed with lower cross syndrome through assessment criteria of Janda muscle testing and assessment

Who cannot join

  • • Having any history of low back pain, spinal trauma,
  • Joint dysfunction in past 3 months
  • Congenital deformities at hip or lumbar region,
  • Recent fracture to related joints in past 6 months
  • Any family history of cardiopulmonary disease
  • Any disease or urogenital tract
Show all 10Show fewer
  • Participants having BMI above 30.
  • Recent history of hepatitis or Fatty liver or
  • Any athlete having high physical activity.
  • History of abdominal, hip or lumbar surgeries in past 3 months

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Al-khumeini Trust Hospital

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Sequential Core Stability Corrective Exercise Approach for Alignment And Muscle Function In Lower Crossed Syndrome

The objective of the study will be to determine the effects of Sequential Core Stability Corrective Exercise Approach for Alignment and Muscle Function in Lower Crossed Syndrome.

Read the detailed description

Lower Crossed Syndrome is one of common postural disorder which occurs due to the muscular imbalance. It refers to specific altered muscle activation and movement patterns along with some postural deviations. Alterations in muscle activation include overactivity of hip flexors and lower back muscles paired underactivity of abdominals and gluteus muscle. This pattern of imbalance creates dysfunction. Postural correction exercise with inner and outer core muscles are necessary. There are different traditional structural approach, functional approach and biomechanics and are presumed to lead to adjustments in the length and strength of local muscles while ignoring other related malalignments and core stability. The objective of the study will be to determine the effects of Sequential Core Stability Corrective Exercise Approach for Alignment and Muscle Function in Lower Crossed Syndrome.

It will be a randomized controlled trial. Sample size will be collected after running the pilot study. The participants will be recruited through convenient sampling technique and then allocated randomly to Groups. Outcome measures will be alignment and muscle function. Pre and post reading and after one month follow-up will be recorded. Data will be analyzed using statistical package for social sciences software version 25. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or nonparametric test will be use within a group or between two groups.

Keywords: Alignment, Core Stability, Diaphragm, Muscular Imbalance, Muscle thickness Pelvic floor.

Conditions
Low Back Pain
Being tested
Control, Sequential Core Stability Corrective Exercise Approach
Keywords
Alignment, Core Stability, Diaphragm, Pelvic floor, Dysfunction
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ControlOther

    Corrective Exercises: Hip Flexor Stretch, Thoracolumbar Extensor Stretch, Abdominal Curl, and Glute Bridge.

  • Sequential Core Stability Corrective Exercise ApproachOther

    Sequential Core Stability Corrective Exercise Approach

    1. Corrective Exercises
    2. Diaphragm Training Program
    3. Pelvic floor Muscle training
    4. Core Stability exercises
    5. Beginning
    6. Progressing
    7. Advanced
Study groups in NCT05505851
Study groupRoleWhat they receive
A: ControlActive comparatorCorrective Exercises: Hip Flexor Stretch, Thoracolumbar Extensor Stretch, Abdominal Curl, and Glute Bridge.
Receives: Other: Control
B: Sequential Core Stability Corrective Exercise ApproachExperimentalSequential Core Stability Corrective Exercise Approach 1. Corrective Exercises 2. Diaphragm Training Program 3. Pelvic floor Muscle training 4. Core Stability exercises
Receives: Other: Sequential Core Stability Corrective Exercise Approach

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Photometry for Pelvic Tilt

    Angle of Pelvic tilt will be measured Through a Reliable and validated camera.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  2. Photometry for Chest Expansion

    Angle of Chest expansion will be measured at Nipple line, Xiphoid level and at waist level, Through a Reliable and validated camera.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  3. Photometry for Cervicothoracic level

    Angle of C7-T1 will be measured Through a Reliable and validated camera.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  4. Photometry for Lumber flexion

    Angle of Lumber curve will be measured Through a Reliable and validated camera.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  5. Diaphragmatic excursion

    To assess the diaphragmatic motion by M-mode US a 2.5-5 megahertz (MHz) phase array will be used.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  6. Levator ani Excursion

    To assess the pelvic floor motion by M-mode US a 2.5-5 megahertz (MHz) array will be used.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  7. Diaphragmatic thickness and thickening

    diaphragmatic thicknesses and thickening will be assessed by B-mode ultrasonography during various respiratory maneuvers

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  8. Levator ani thickness and thickening

    Levator ani thicknesses and thickening will be assessed by B-mode ultrasonography during various respiratory maneuvers

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  9. Core stability

    It will be measured by Pressure biofeedback unit for the transverse abdomens.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

Secondary outcomes (3)
  1. Forced Vital Capacity (FVC)

    Pulmonary function test through spirometer, It will be measured by digital spirometer.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  2. Forced Expiratory Volume per second FEV1

    Pulmonary function test through spirometer, It will be measured by digital spirometer.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

  3. Ratio of FEV1/ FVC

    Pulmonary function test through spirometer, It will be measured by digital spirometer.

    Measured: Pre (0th week), Post (6th week), (12th week) Follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Aug 2022
  2. Study start10 Feb 2024
  3. Primary completion1 Dec 2025
  4. Study completion1 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
2
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05505851
Sponsor's protocol ID
REC/RCR & AHS/22/1104
Acronym
SCSCRLCS
Status last verified
Dec 2025
First submitted
23 May 2022
Last updated
15 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Sequential Core Stability Corrective Exercise Approach in people with Low Back Pain, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 15 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Photometry for Pelvic Tilt (time frame: Pre (0th week), Post (6th week), (12th week) Follow-up). The study lists 9 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Dec 2025.

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SCSCRLCS Clinical Trial NCT05505851 | AzTrials