Skip to content

Comparison of High-Intensity Interval Training With Moderate-Intensity Continuous Training in Chronic Non-Specific Low Back Pain Patients

Comparison of High-Intensity Interval Training With Moderate-Intensity Connuous Training In Chronic Non-Specific Low Back Pain Patients: Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07645859
Enrollment
80
Registered
2026-06-12
Start date
2026-05-14
Completion date
2026-12-01
Last updated
2026-06-12

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

Conditions

Chronic Non-Specific Low Back Pain

Keywords

High-Intensity Interval Training, Moderate-Intensity Continuous Training, Chronic Non-Specific Low Back Pain, Aerobic, Heart rate, Body composition, Anaerobic

Brief summary

The goal of this clinical trial is to compare the HIIT with MICT in chronic non-specific low back pain patients. The main questions it aims to answer are: * The broad aim of the study is to compare HIIT with MICT in pain reduction in chronic non-specific low back pain patients. * The purpose of this research is to compare HIIT with MICT on disability and quality of life among chronic non-specific low back pain patients. * It also attempts to investigate the relationship between the baseline attributes and outcome variables. Researcher will compare the HIIT to MICT to see the effects on CNSLBP Participants will be: * Allocated to HIIT or MICT group for 6 weeks. * Assessed pre and post intervention. * Continuously monitored during treatment sessions.

Interventions

OTHERBrisk walk and jog

High-Intensity Interval Training

OTHERNormal walk

Moderate-Intensity Continuous Training

Sponsors

Dow University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 48 Years
Healthy volunteers
No

Inclusion criteria

* Referred patients of back pain persisting for \> 12 weeks with no identifiable specific cause or underlying pathology from DUH OPD who meet the eligibility criteria. * Age group 20-48 with either gender. * NPRS score ranging between 3 and 5 (mild to moderate). * Modified ODI score is mild to moderate.

Exclusion criteria

* Any client with a specific cause of LBP (neurological problems, fractures, malignancy, infections, or rheumatic diseases such as RA or ankylosing spondylitis). * Any client with cardiopulmonary problems (recent myocardial infarction, uncontrolled hypertension, asthma, COPD). * Any client with musculoskeletal disorders \[injuries limiting exercises, spine injuries, recent trauma (fracture), scoliosis by Forward Adam's test\]. * Any client with metabolic conditions (thyroid problems, uncontrolled diabetes). * Pregnancy / first 3-6 months postpartum. * Recent surgery.

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Score (NPRS)6 weeksLow back pain persisting for \> 12 weeks with no identifiable specific cause or underlying pathology Score: Mild to moderate (3-5)

Secondary

MeasureTime frameDescription
Modified Oswestry Disability Index for disability6 weeksDisability percentage derived from 10-item ODI scores 20-40% considered mild to moderate and eligible.
Short Form-12 for Quality of Life6 weeks
Modified Bruce Treadmill protocol for CV endurance6 weeks
Bioelectrical Impedance Analysis (BIA) for body composition6 weeks
height and weight for Body Mass Index6 weeks
Waist Hip Ratio for fat distribution6 weeks

Countries

Pakistan

Contacts

CONTACTAriba Dr. Ariba Sohail (PT)
aribasohail123@gmail.com+923480218683
PRINCIPAL_INVESTIGATORAriba Sohail

Dow University of Health Sciences

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026