Skip to content

Combined Effects of Yoga and Pilates versus Conventional Exercises on Pain, Core Strength, fear of movement, and Disability in Patients with Non-Specific Low Back Pain for longer time: A Randomized Controlled Trial

Combined Effects of Yoga and Pilates versus Conventional Exercises on Pain, Core Strength, Kinesiophobia, and Disability in Patients with Chronic Non-Specific Low Back Pain: A Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/102567
Enrollment
60
Registered
2026-01-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: Combined Yoga and Pilates: Baseline assessment and evaluation same as the Comparator group. The intervention will consist of supervised combined Yoga Pilates exercises conducted five se
3 repetitions with 20 30 second holds), Ardha or Paripurna Navasana (5 repetitions, 20 seconds each), Adho Mukha Svanasana (5 repetitions, 20 seconds each), Utkatasana (5 repetitions, 20 seconds each)

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The inclusion criteria for this study will include adults aged 18 60 years who are diagnosed with chronic non-specific low back pain, defined as pain persisting for at least 12 weeks, and who are willing to provide informed consent and comply with the prescribed exercise program. The inclusion criteria for this study will include adults aged 18 60 years who are diagnosed with chronic non-specific low back pain, defined as pain persisting for at least 12 weeks, and who are willing to provide informed consent and comply with the prescribed exercise program.

Exclusion criteria

Exclusion criteria: The exclusion criteria will include individuals with specific spinal pathologies such as disc herniation with radiculopathy, spinal stenosis, osteoporosis, or neoplasm, those with a history of spinal surgery within the past year, participants presenting with neurological deficits or red-flag signs, pregnant women, and individuals with severe cardiorespiratory conditions or any other contraindications to exercise.

Design outcomes

Primary

MeasureTime frame
Numeric Pain Rating Scale (NPRS)Timepoint: out come will be taken before intervention and after intervention which is of 3 week of exercise protocol so immediatly after protocol

Secondary

MeasureTime frame
Pressure Biofeedback for core strength evalutaion.Timepoint: Outcome measures will be assessed at two time points: baseline, after participant enrollment and after intervention completion.;TAMPA scale for kinesiophobia to assess fear of movement and reinjury.Timepoint: Outcome measures will be assessed at two time points: baseline, after participant enrollment and after intervention completion.;Ronald-Morris Disability Questionnaire (RMDQ) to assess the impact of pain on daily activity and functional mobility.Timepoint: Outcome measures will be assessed at two time points: baseline, after participant enrollment and after intervention completion.

Countries

India

Contacts

Public ContactDr Bhavya Soni

K.M. Patel Institute of Physiotherapy

bhavyavsoni8@gmail.com8866505004

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026