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Clinical Trials/NCT07645859
NCT07645859RecruitingNot Applicable

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

Dow University of Health Sciences1 site in 1 country80 target enrollmentStarted: May 14, 2026Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
80
Locations
1
Study OverviewStudy DesignEligibility CriteriaInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 48 Years (Adult)
Sex
All
Accepts 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.

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Ariba Sohail (PT)

Principal Investigator

Dow University of Health Sciences

Study Sites (1)

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