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EFFECTS OF SPINAL MANIPULATION ON THORACIC SPINAL PAIN

EFFECTS OF SPINAL MANIPULATION VERSUS ROUTINE PHYSICAL THERAPY ON THORACIC SPINAL PAIN;A RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190327043125N1
Enrollment
100
Registered
2019-06-08
Start date
2640-06-21
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Thoracic Spinal Pain effecting Quality of Life. Pain in thoracic spine

Interventions

Intervention 1: Intervention group:Subjects in experimental group will be managed with spinal manipulative therapy (a single attempt of high-velocity low-amplitude thrust in prone position) & ergonom

Sponsors

Services Hospital Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: Only patients who will receive a diagnosis of thoracic spine pain from the researcher will be accepted into the study. Diagnosis will be made by questioning and examining the subject .• Age between 40 and 60 years Midline back pain Mobility deficit in thoracic range of motion Pain with compression into spine extension Patients without any known cause of TSP

Exclusion criteria

Exclusion criteria: Patient with neurological signs & symptoms Osteoporosis Severe spinal deformity Any systemic disease e.g. cardiovascular or neurological etc Traumatic history and any other red flags of spinal pain

Design outcomes

Primary

MeasureTime frame
Thoracic spine pain intesity. Timepoint: before and after treatment session and 8 & 12 weeks after treatment. Method of measurement: visual analogue scale to measure pain.

Secondary

MeasureTime frame
Chest expansion. Timepoint: before and after intervention and 8, 12 weeks after intervention. Method of measurement: measuring tape.;Range of motion. Timepoint: before and after intervention and 8, 12 weeks after intervention. Method of measurement: goniometer.;Quality of Life. Timepoint: before and after intervention and 8, 12 weeks after intervention. Method of measurement: Quality of Life questionnaire.;Blood pressure. Timepoint: before and after intervention and 8, 12 weeks after intervention. Method of measurement: digital sphygmomanometer.;Heart rate. Timepoint: before and after intervention and 8, 12 weeks after intervention. Method of measurement: pulse oximeter.

Countries

Pakistan

Contacts

Public ContactDr Ashfaq Ahmed

The University of Lahore

ashfaq.ahmad@uipt.uol.edu.pk+92 42 111 865 865

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 10, 2026