NCT07467070

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

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Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable low-back-pain

Timeline
Completed

Started Mar 2026

Shorter than P25 for not_applicable low-back-pain

Geographic Reach
1 country

1 active site

Status
recruiting

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

Completed
Same day until next milestone

Study Start

First participant enrolled

March 3, 2026

Completed
9 days until next milestone

First Posted

Study publicly available on registry

March 12, 2026

Completed
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 9, 2026

Completed
11 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 20, 2026

Completed
Last Updated

March 12, 2026

Status Verified

March 1, 2026

Enrollment Period

1 month

First QC Date

March 3, 2026

Last Update Submit

March 7, 2026

Conditions

Keywords

Pilatescore strengthflexibilitypostural correctionyoung individualsNon-specific low backachelow back pain

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

EXPERIMENTAL

Participants will perform Pilates intervention targeting the posture, core strength and flexibility along with the conventional therapy.

Behavioral: PilatesBehavioral: conventional therapy

Conventional Group

ACTIVE COMPARATOR

Participants will perform conventional therapy for non-specific low backache.

Behavioral: conventional therapy

Interventions

PilatesBEHAVIORAL

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.

Pilates Group

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.

Conventional GroupPilates Group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

MeSH Terms

Conditions

Low Back Pain

Interventions

Exercise Movement Techniques

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Physical Therapy ModalitiesTherapeutics

Central Study Contacts

Muqaddus Fatima, Doctor of Physical Therapy

CONTACT

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

Locations