Effectiveness of Pilates on Postural Correction, Core Strength and Flexibility in Younger Individuals With Non-specific Low Backache
Effects of Pilates on Postural Correction, Core Strength and Flexibility in Young Individuals With Non-Specific Low Backache
1 other identifier
interventional
50
1 country
1
Brief Summary
The aim of this clinical trial is to study the effects of Pilates intervention versus conventional therapy on postural correction, core strength and flexibility in young individuals with complaint of non-specific low backache. The main question is whether the Pilates has better improvement as compared to the conventional therapy on postural correction, core strength and flexibility moreover to compare the effectiveness of two intervention. Participants of age 18-25 years and with complaint of non-specific low backache will be recruited. 50 participants will be enrolled. Participants will perform Pilates and conventional therapy for 3 times per week for six weeks. Participants will be randomly allocated to two groups and assessor blinding will be done to take baseline assessment. Assessor blinding is done to minimize biasness. Pre and Post assessments will be taken by the assessor. SPSS will be used for the analysis of the data.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable low-back-pain
Started Mar 2026
Shorter than P25 for not_applicable low-back-pain
1 active site
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 3, 2026
CompletedStudy Start
First participant enrolled
March 3, 2026
CompletedFirst Posted
Study publicly available on registry
March 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 9, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 20, 2026
CompletedMarch 12, 2026
March 1, 2026
1 month
March 3, 2026
March 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Posture
Assessed by using Postural Habit and Awareness Scale. It is based on a Likert scale. The maximum score is of 95. The higher score indicate better postural awareness and healthier postural habits, while lower score suggest poor postural awareness and faulty postural behaviors.
Baseline and 6th week
Core Strength
Assessed by using Front Plank Test. Time duration will be noted by maintaining the correct alignment of the body. The higher Score indicates the better core strength.
Baseline and 6th week
Flexibility
Assessed by using V Sit and Reach Test. Distance will be noted in inches. The higher score indicates the better flexibility.
Baseline and 6th week
Study Arms (2)
Pilates Group
EXPERIMENTALParticipants will perform Pilates intervention targeting the posture, core strength and flexibility along with the conventional therapy.
Conventional Group
ACTIVE COMPARATORParticipants will perform conventional therapy for non-specific low backache.
Interventions
Participants will perform supervised mat-based Pilates exercise program designed to improve posture, core strength and flexibility. This intervention will be only applied to experimental group. Pilates is a mind body exercise system that emphasize on controlled breathing pattern with proper alignment of the body. Intervention will be applied for six weeks.
Participants will receive structured and supervised conventional therapy aiming at posture, core strength and flexibility. It consists of standardized therapeutic exercises commonly used in clinical practice and clinical guidelines. Conventional Therapy will be applied for six weeks to both the groups.
Eligibility Criteria
You may qualify if:
- Age 18-25
- Non-specific low backache of pain severity less than and equal to 5/10 on Brief Pain Inventory Scale
- Ability to attend complete six-week program
- Both genders
You may not qualify if:
- prior history of trauma, fracture, spinal stenosis, severe comorbidities, spinal surgery and neurological disorders
- Individuals suffering from specific causes of low backache like Infection and pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Health Sciences Lahore
Lahore, Punjab Province, 54600, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 3, 2026
First Posted
March 12, 2026
Study Start
March 3, 2026
Primary Completion
April 9, 2026
Study Completion
April 20, 2026
Last Updated
March 12, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share