Effectiveness of Pilates on Postural Correction, Core Strength and Flexibility in Younger Individuals With Non-specific Low Backache

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-25
SponsorUniversity of Health Sciences Lahore

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial design

Design model

Parallel

Treatments tested in this trial

  • Pilates

    Behavioral

    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.

  • conventional therapy

    Behavioral

    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.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Pilates GroupExperimental treatment 2 interventions
Group B: Conventional GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

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.

Time frame
Baseline and 6th week
2

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.

Time frame
Baseline and 6th week
3

Flexibility

Assessed by using V Sit and Reach Test. Distance will be noted in inches. The higher score indicates the better flexibility.

Time frame
Baseline and 6th week

Secondary outcomes

Other outcomes

Sponsors and contacts

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