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Kaltenborn Mobilization With and Without Proprioceptive Neuromuscular Facilitation Technique in Low Back Pain.

Effects of Kaltenborn Mobilization With and Without Proprioceptive Neuromuscular Facilitation Technique on Pain, Range of Motion and Function in Patients With Chronic Non Specific Low Back Pain.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07403110
Enrollment
50
Registered
2026-02-11
Start date
2025-10-14
Completion date
2025-12-05
Last updated
2026-02-11

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

Conditions

Non-specific Chronic Low Back Pain

Keywords

disability, mobility, back pain

Brief summary

The study was conducted to determine the effects of Kaltenborn mobilization with and without proprioceptive neuromuscular facilitation technique on pain, range of motion and function in patients with chronic non-specific low back pain.

Interventions

Kaltenborn mobilization was applied to the lumbar spine area in the dorsal direction . Patient was positioned in flexion , side bending and rotation to the right and glide was applied in dorsal direction. Similar glide was given to patient in extension, side bending and rotation to the right. These techniques were performed for 3 days per week for 6 consecutive weeks.

PNF Hold Relax technique was performed on lumbar spine to increase the extensibility of the surrounding muscles after a maximal response. These techniques were performed for 3 days per week for 6 consecutive weeks.

Hotpack for 10 mins was applied with Tens at a burst mode with pulse width 200 microsec, frequency 100 Hz, burst frequency 2 Hz for 10 mins. Ultrasound was applied for 10 mins, stretching of calf, hamstrings and gluteals along with back strengthening.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Age range of 25 to 45 * Pain lasting for more than 3 months * Score between 2 to 7 in NPRS * Score of greater than 20 in ODI * Pain localized between the level below the ribs at the posterior side and above the level of buttocks.

Exclusion criteria

* Any neoplasm involving back * Radiating pain * Metabolic disorders like osteoporosis * Pregnancy * Acute infection * Prior orthopedic surgeries * Acute trauma

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating ScaleFrom enrollment to the end of treatment at 6 weeks.Numeric Pain Rating scale is used to measure intensity of pain. It ranges from 0 to 10 where 0 represents no pain, 1-3 represents mild pain, 4-6 represents moderate pain and 7-10 shows severe pain.
Oswestry Disability IndexFrom enrollment to the end of treatment at 6 weeksOswetry Disability index is a questionnaire consisting of 10 questions used to asses functional disability in patients with low back pain. In this scale, 0-20% = minimal disability, 21-40% = moderate disability, 41-60% = severe disability, 61-80% = crippled and 81-100% = bedbound.

Secondary

MeasureTime frameDescription
ROM of Lumbar Spine ( Extension)From enrollment to the end of treatment at 6 weeksChanges in lumbar extension range of motion was measured using goniometer at baseline to the end of treatment at 6 weeks.
ROM Lumbar spine (Flexion)From enrollment to end of treatment at 6 weeks.Changes in lumbar flexion range of motion was measured using goniometer at baseline and at the end of 6 weeks.

Countries

Pakistan

Contacts

PRINCIPAL_INVESTIGATORShakil ur Rehman, Ph.D

Riphah International University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026