StrokeNCT07902310
Effects of Contralateral Gravity Eliminated Gluteus Medius and Ipsilateral Quadratus Lumborum Strengthening on Pelvic Alignment, Balance and Functional Mobility on Subacute Stroke Patients
A study testing Contralateral Gravity-Eliminated Gluteus Medius Strengthening, Quadratus Lumborum Strengthening Group and Conventional Physiotherapy in people with Stroke, run by Lahore University of Biological and Applied Sciences at 1 site in Pakistan.
Trial summary
This study aims to compare the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening, both combined with conventional physiotherapy, on pelvic alignment, balance, and functional mobility in patients with subacute stroke. Read more about this study
- Who is it for?
- Ages 45 to 65 years
- Conditions the study is for
- Stroke
- What is being tested?
- Contralateral Gravity-Eliminated Gluteus Medius Strengthening, Quadratus Lumborum Strengthening Group and Conventional Physiotherapy
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 sitePakistan
- Study dates
- 15 Aug 2026to 30 Jan 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 45 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Patients aged 45-65 years. Patients with a first-ever stroke occurring 1-6 months before enrollment (subacute stroke).
- Patients classified within Brunnstrom Recovery Stages III-V. Medically stable patients who are able to follow simple verbal commands. Patients able to stand independently or with minimal assistance. Patients with a Berg Balance Scale (BBS) score below 45 out of 56.
Who cannot join
- Patients with a history of recurrent stroke. Patients with severe cognitive impairment. Patients with other neurological disorders that may affect rehabilitation outcomes.
- Patients with severe lower-limb musculoskeletal conditions. Patients with severe spasticity, defined as a Modified Ashworth Scale (MAS) score greater than 3, according to the study protocol.
- Patients with uncontrolled cardiovascular or respiratory disease. Patients with severe visual or vestibular impairment affecting balance. Patients unable to stand even with assistance. Patients participating in another rehabilitation research study during the study period.
- -
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Pakistan1 site, 1 recruiting
- Recruiting
Alfalah Medical Center
Lahore, Punjab Province
Dr Sharafat Ali, DPT, 03064019521, physiosharafat@gmail.com
About this study
This study aims to compare the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening, both combined with conventional physiotherapy, on pelvic alignment, balance, and functional mobility in patients with subacute stroke. This single-blinded, two-arm, parallel-group randomized clinical trial will be conducted at the Department of Physical Therapy Rehabilitation, Alfalah Medical Center, Lahore, Pakistan. A total of 40 participants aged 45-60 years with a first-ever stroke occurring 1-6 months before enrollment will be recruited and randomly allocated to two groups. Group A will receive 30 minutes of conventional physiotherapy followed by 20 minutes of contralateral gravity-eliminated gluteus medius strengthening, while Group B will receive 30 minutes of conventional physiotherapy followed by 20 minutes of ipsilateral quadratus lumborum strengthening. Both groups will receive treatment three times per week for six weeks. The primary outcome measures will include pelvic alignment assessed using the Palpation Meter (PALM), balance assessed using the Berg Balance Scale (BBS), and functional mobility assessed using the Timed Up and Go (TUG) test. All outcome measures will be assessed at baseline, immediately after the six-week intervention, and at week 12 to evaluate changes following treatment and at follow-up. The study will compare outcomes between the two groups to determine the relative effectiveness of the two targeted strengthening approaches when combined with conventional physiotherapy in patients with subacute stroke.
Read the detailed description
This study aims to compare the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening, both combined with conventional physiotherapy, on pelvic alignment, balance, and functional mobility in patients with subacute stroke. This study will be conducted as a single-blinded, two-arm, parallel-group randomized clinical trial at the Department of Physical Therapy Rehabilitation, Alfalah Medical Center, Lahore, Pakistan. The planned study duration is 12 months following synopsis approval. A total of 40 participants aged 45-60 years with a first-ever stroke occurring 1-6 months before enrollment will be recruited through convenience sampling and randomly allocated in a 1:1 ratio using a computer-generated random sequence and sequentially numbered opaque sealed envelopes. Eligible participants will be medically stable, demonstrate Brunnstrom Recovery Stages III-V, be able to follow simple verbal commands, be able to stand independently or with minimal assistance, and have a Berg Balance Scale score below 45 out of 56. Participants with recurrent stroke, severe cognitive impairment, other neurological disorders, severe lower-limb musculoskeletal conditions, severe lower-limb spasticity defined as a Modified Ashworth Scale score greater than 3, uncontrolled cardiovascular or respiratory disease, severe visual or vestibular impairment affecting balance, inability to stand even with assistance, or participation in another rehabilitation research study during the study period will be excluded. Participants will be divided into two groups. Group A will receive 30 minutes of conventional physiotherapy combined with 20 minutes of contralateral gravity-eliminated gluteus medius strengthening per session, three times per week for six weeks. The strengthening program will include supported gravity-eliminated hip abduction exercises, active-assisted and active muscle activation, pelvic stabilization, controlled hip abduction with sustained holds, and progression according to the participant's motor control and tolerance. Group B will receive the same 30-minute conventional physiotherapy program combined with 20 minutes of ipsilateral quadratus lumborum strengthening per session, three times per week for six weeks. Exercises will include isometric quadratus lumborum activation, side-lying pelvic hiking, controlled pelvic lowering, and progressive trunk and pelvic stabilization exercises in appropriate positions according to the participant's abilities and tolerance. Conventional physiotherapy will be provided to both groups and will include range-of-motion exercises, trunk and pelvic control activities, weight shifting, balance training, and gait-related exercises based on the Bobath Concept, Brunnstrom Approach, and conventional physiotherapy principles. The outcome assessor will be blinded to group allocation. All three outcome measures will be considered primary outcomes. Pelvic alignment will be assessed using the Palpation Meter (PALM), balance will be assessed using the Berg Balance Scale (BBS), and functional mobility will be assessed using the Timed Up and Go (TUG) test. The PALM will be used to measure pelvic tilt in degrees, the BBS will assess functional balance using 14 tasks with a maximum total score of 56, and the TUG will measure the time required to stand from a chair, walk three metres, turn, return, and sit down. All outcome measures will be assessed at baseline, immediately after completion of the six-week intervention, and at week 12 to evaluate changes following treatment and at follow-up. The results will be compared between the two groups to determine the relative effectiveness of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening when combined with conventional physiotherapy in improving pelvic alignment, balance, and functional mobility in patients with subacute stroke.
- Conditions
- Stroke
- Being tested
- Contralateral Gravity-Eliminated Gluteus Medius Strengthening, Quadratus Lumborum Strengthening Group, Conventional Physiotherapy
- Keywords
- Subacute Stroke, Gluteus Medius Strengthening, Quadratus Lumborum Strengthening, Conventional Physiotherapy , Pelvic Alignment
- Medical subject headings
- Stroke
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Contralateral Gravity-Eliminated Gluteus Medius StrengtheningBehavioural
Participants will receive 20 minutes of contralateral gravity-eliminated gluteus medius strengthening per session, three times per week for six weeks. Exercises will focus on selective gluteus medius activation, supported hip abduction in gravity-eliminated positions, and pelvic stabilization. Exercise difficulty will be adjusted according to participants' motor control and tolerance
Quadratus Lumborum Strengthening GroupBehavioural
Group B participants will receive conventional physiotherapy combined with ipsilateral quadratus lumborum strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted quadratus lumborum strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving quadratus lumborum activation, trunk stability, and pelvic control.
Conventional PhysiotherapyBehavioural
Participants will receive 30 minutes of conventional physiotherapy per session, three times per week for six weeks. Treatment will include range-of-motion exercises, trunk and pelvic control activities, weight shifting, balance training, and gait-related exercises based on the Bobath Concept, Brunnstrom Approach, and conventional physiotherapy principles.
| Study group | Role | What they receive |
|---|---|---|
| Experimental: Contralateral Gravity-Eliminated Gluteus Medius Strengthening Group | Experimental | Group A participants will receive conventional physiotherapy combined with contralateral gravity-eliminated gluteus medius strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted gluteus medius strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving gluteus medius activation, pelvic control, and lumbopelvic stability through supported gravity-eliminated exercises. Receives: Behavioral: Contralateral Gravity-Eliminated Gluteus Medius Strengthening; Behavioral: Conventional Physiotherapy |
| Quadratus Lumborum Strengthening Group | Active comparator | Group B participants will receive conventional physiotherapy combined with ipsilateral quadratus lumborum strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted quadratus lumborum strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving quadratus lumborum activation, trunk stability, and pelvic control. Receives: Behavioral: Quadratus Lumborum Strengthening Group; Behavioral: Conventional Physiotherapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Pelvic Alignment (PALM)
Pelvic alignment will be assessed using the Palpation Meter (PALM), which measures pelvic inclination in degrees using standardized positioning and palpation of relevant pelvic landmarks. Changes in pelvic tilt will be evaluated to determine the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening combined with conventional physiotherapy.
Measured: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Berg Balance Scale (BBS)
Functional balance will be assessed using the Berg Balance Scale (BBS), which consists of 14 functional tasks, each scored from 0 to 4, with a maximum total score of 56. Higher scores indicate better balance performance. Changes in total BBS scores will be compared between the two intervention groups to evaluate improvements in functional balance.
Measured: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Timed Up and Go (TUG)
Functional mobility will be assessed using the Timed Up and Go (TUG) test. Participants will be instructed to stand up from a chair, walk 3 metres, turn around, return to the chair, and sit down. The time required to complete the test will be recorded in seconds. A shorter completion time indicates better functional mobility. Changes in TUG completion time will be compared between the two intervention groups.
Measured: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Oct 2026
- Study start15 Aug 2026
- Primary completion30 Dec 2026 (estimated)
- Study completion30 Jan 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for StrokeStudies of the same condition, open and under way.
- More trials run by Lahore University of Biological and Applied SciencesThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Prof. Dr. Shoaib Waqas, Lahore University of Biological and Applied Sciences
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07902310
- Sponsor's protocol ID
- UBAS/ERB/26/07/083
- Status last verified
- Oct 2026
- First submitted
- 21 Oct 2026
- Last updated
- 28 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Contralateral Gravity Eliminated Gluteus Medius and Ipsilateral Quadratus Lumborum Strengthening on Pelvic Alignment, Balance and Functional Mobility on Subacute Stroke Patients
- ClinicalTrials.gov ID
- NCT07902310
- Acronym / sponsor ID
- UBAS/ERB/26/07/083
- Conditions
- Stroke
- Keywords
- Subacute Stroke, Gluteus Medius Strengthening, Quadratus Lumborum Strengthening, Conventional Physiotherapy , Pelvic Alignment
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Lahore University of Biological and Applied SciencesUniversity, hospital or other
- Study start
- 15 Aug 2026 (actual)
- Primary completion
- 30 Dec 2026 (estimated)
- Study completion
- 30 Jan 2027 (estimated)
- First posted
- 28 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to compare the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening, both combined with conventional physiotherapy, on pelvic alignment, balance, and functional mobility in patients with subacute stroke. This single-blinded, two-arm, parallel-group randomized clinical trial will be conducted at the Department of Physical Therapy Rehabilitation, Alfalah Medical Center, Lahore, Pakistan. A total of 40 participants aged 45-60 years with a first-ever stroke occurring 1-6 months before enrollment will be recruited and randomly allocated to two groups. Group A will receive 30 minutes of conventional physiotherapy followed by 20 minutes of contralateral gravity-eliminated gluteus medius strengthening, while Group B will receive 30 minutes of conventional physiotherapy followed by 20 minutes of ipsilateral quadratus lumborum strengthening. Both groups will receive treatment three times per week for six weeks. The primary outcome measures will include pelvic alignment assessed using the Palpation Meter (PALM), balance assessed using the Berg Balance Scale (BBS), and functional mobility assessed using the Timed Up and Go (TUG) test. All outcome measures will be assessed at baseline, immediately after the six-week intervention, and at week 12 to evaluate changes following treatment and at follow-up. The study will compare outcomes between the two groups to determine the relative effectiveness of the two targeted strengthening approaches when combined with conventional physiotherapy in patients with subacute stroke.
Detailed description
This study aims to compare the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening, both combined with conventional physiotherapy, on pelvic alignment, balance, and functional mobility in patients with subacute stroke. This study will be conducted as a single-blinded, two-arm, parallel-group randomized clinical trial at the Department of Physical Therapy Rehabilitation, Alfalah Medical Center, Lahore, Pakistan. The planned study duration is 12 months following synopsis approval. A total of 40 participants aged 45-60 years with a first-ever stroke occurring 1-6 months before enrollment will be recruited through convenience sampling and randomly allocated in a 1:1 ratio using a computer-generated random sequence and sequentially numbered opaque sealed envelopes. Eligible participants will be medically stable, demonstrate Brunnstrom Recovery Stages III-V, be able to follow simple verbal commands, be able to stand independently or with minimal assistance, and have a Berg Balance Scale score below 45 out of 56. Participants with recurrent stroke, severe cognitive impairment, other neurological disorders, severe lower-limb musculoskeletal conditions, severe lower-limb spasticity defined as a Modified Ashworth Scale score greater than 3, uncontrolled cardiovascular or respiratory disease, severe visual or vestibular impairment affecting balance, inability to stand even with assistance, or participation in another rehabilitation research study during the study period will be excluded. Participants will be divided into two groups. Group A will receive 30 minutes of conventional physiotherapy combined with 20 minutes of contralateral gravity-eliminated gluteus medius strengthening per session, three times per week for six weeks. The strengthening program will include supported gravity-eliminated hip abduction exercises, active-assisted and active muscle activation, pelvic stabilization, controlled hip abduction with sustained holds, and progression according to the participant's motor control and tolerance. Group B will receive the same 30-minute conventional physiotherapy program combined with 20 minutes of ipsilateral quadratus lumborum strengthening per session, three times per week for six weeks. Exercises will include isometric quadratus lumborum activation, side-lying pelvic hiking, controlled pelvic lowering, and progressive trunk and pelvic stabilization exercises in appropriate positions according to the participant's abilities and tolerance. Conventional physiotherapy will be provided to both groups and will include range-of-motion exercises, trunk and pelvic control activities, weight shifting, balance training, and gait-related exercises based on the Bobath Concept, Brunnstrom Approach, and conventional physiotherapy principles. The outcome assessor will be blinded to group allocation. All three outcome measures will be considered primary outcomes. Pelvic alignment will be assessed using the Palpation Meter (PALM), balance will be assessed using the Berg Balance Scale (BBS), and functional mobility will be assessed using the Timed Up and Go (TUG) test. The PALM will be used to measure pelvic tilt in degrees, the BBS will assess functional balance using 14 tasks with a maximum total score of 56, and the TUG will measure the time required to stand from a chair, walk three metres, turn, return, and sit down. All outcome measures will be assessed at baseline, immediately after completion of the six-week intervention, and at week 12 to evaluate changes following treatment and at follow-up. The results will be compared between the two groups to determine the relative effectiveness of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening when combined with conventional physiotherapy in improving pelvic alignment, balance, and functional mobility in patients with subacute stroke.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Experimental: Contralateral Gravity-Eliminated Gluteus Medius Strengthening Group | Experimental | Behavioral: Contralateral Gravity-Eliminated Gluteus Medius Strengthening, Behavioral: Conventional PhysiotherapyGroup A participants will receive conventional physiotherapy combined with contralateral gravity-eliminated gluteus medius strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted gluteus medius strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving gluteus medius activation, pelvic control, and lumbopelvic stability through supported gravity-eliminated exercises. |
| Quadratus Lumborum Strengthening Group | Active comparator | Behavioral: Quadratus Lumborum Strengthening Group, Behavioral: Conventional PhysiotherapyGroup B participants will receive conventional physiotherapy combined with ipsilateral quadratus lumborum strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted quadratus lumborum strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving quadratus lumborum activation, trunk stability, and pelvic control. |
Who may qualify
- Ages
- 45 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Patients aged 45-65 years. Patients with a first-ever stroke occurring 1-6 months before enrollment (subacute stroke).
- Patients classified within Brunnstrom Recovery Stages III-V. Medically stable patients who are able to follow simple verbal commands. Patients able to stand independently or with minimal assistance. Patients with a Berg Balance Scale (BBS) score below 45 out of 56.
Key exclusion criteria (4 listed)
- Patients with a history of recurrent stroke. Patients with severe cognitive impairment. Patients with other neurological disorders that may affect rehabilitation outcomes.
- Patients with severe lower-limb musculoskeletal conditions. Patients with severe spasticity, defined as a Modified Ashworth Scale (MAS) score greater than 3, according to the study protocol.
- Patients with uncontrolled cardiovascular or respiratory disease. Patients with severe visual or vestibular impairment affecting balance. Patients unable to stand even with assistance. Patients participating in another rehabilitation research study during the study period.
- -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Contralateral Gravity-Eliminated Gluteus Medius StrengtheningParticipants will receive 20 minutes of contralateral gravity-eliminated gluteus medius strengthening per session, three times per week for six weeks. Exercises will focus on selective gluteus medius activation, supported hip abduction in gravity-eliminated positions, and pelvic stabilization. Exercise difficulty will be adjusted according to participants' motor control and tolerance | Behavioural | Experimental: Contralateral Gravity-Eliminated Gluteus Medius Strengthening Group |
| Quadratus Lumborum Strengthening GroupGroup B participants will receive conventional physiotherapy combined with ipsilateral quadratus lumborum strengthening for six weeks. Each session will include 30 minutes of conventional physiotherapy and 20 minutes of targeted quadratus lumborum strengthening. Sessions will be conducted three times per week for six weeks, for a total of 18 supervised sessions. The program will focus on improving quadratus lumborum activation, trunk stability, and pelvic control. | Behavioural | Quadratus Lumborum Strengthening Group |
| Conventional PhysiotherapyParticipants will receive 30 minutes of conventional physiotherapy per session, three times per week for six weeks. Treatment will include range-of-motion exercises, trunk and pelvic control activities, weight shifting, balance training, and gait-related exercises based on the Bobath Concept, Brunnstrom Approach, and conventional physiotherapy principles. | Behavioural | Experimental: Contralateral Gravity-Eliminated Gluteus Medius Strengthening Group, Quadratus Lumborum Strengthening Group |
Primary outcome
Pelvic Alignment (PALM)
Time frame: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Pelvic alignment will be assessed using the Palpation Meter (PALM), which measures pelvic inclination in degrees using standardized positioning and palpation of relevant pelvic landmarks. Changes in pelvic tilt will be evaluated to determine the effects of contralateral gravity-eliminated gluteus medius strengthening and ipsilateral quadratus lumborum strengthening combined with conventional physiotherapy.
Berg Balance Scale (BBS)
Time frame: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Functional balance will be assessed using the Berg Balance Scale (BBS), which consists of 14 functional tasks, each scored from 0 to 4, with a maximum total score of 56. Higher scores indicate better balance performance. Changes in total BBS scores will be compared between the two intervention groups to evaluate improvements in functional balance.
Timed Up and Go (TUG)
Time frame: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.
Functional mobility will be assessed using the Timed Up and Go (TUG) test. Participants will be instructed to stand up from a chair, walk 3 metres, turn around, return to the chair, and sit down. The time required to complete the test will be recorded in seconds. A shorter completion time indicates better functional mobility. Changes in TUG completion time will be compared between the two intervention groups.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Contralateral Gravity-Eliminated Gluteus Medius Strengthening, Quadratus Lumborum Strengthening Group and Conventional Physiotherapy in people with Stroke, run by Lahore University of Biological and Applied Sciences 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 2 inclusion and 4 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: looking for participants now, as of the sponsor's last update on 28 Oct 2026. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Prof.Dr Shoaib Waqas, PHD (+92 302 4552109, shoaib.waqas@ubas.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Pelvic Alignment (PALM) (time frame: Baseline, immediately after the 6-week intervention (Week 6), and at Week 12 follow-up.). The study lists 3 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 28 Oct 2026.