NCT05853926

Brief Summary

To determine the effectiveness of spinal manipulation with laser therapy versus dry needling for pain, disability and fear of movement in chronic low backache

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
54

participants targeted

Target at P25-P50 for not_applicable low-back-pain

Timeline
Completed

Started Apr 2023

Shorter than P25 for not_applicable low-back-pain

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 18, 2023

Completed
14 days until next milestone

Study Start

First participant enrolled

April 1, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

May 11, 2023

Completed
21 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2023

Completed
Last Updated

May 11, 2023

Status Verified

May 1, 2023

Enrollment Period

2 months

First QC Date

March 18, 2023

Last Update Submit

May 2, 2023

Conditions

Low Back Pain

Outcome Measures

Primary Outcomes (1)

  • Oswestry Disability Index scale

    6 Months

Study Arms (2)

Spinal Manipulation With Laser Therapy

EXPERIMENTAL
Diagnostic Test: Spinal Manipulation With Laser Therapy

Dry Needling

OTHER
Diagnostic Test: Dry Needling

Interventions

Spinal Manipulation With Laser TherapyDIAGNOSTIC_TEST

Spinal Manipulation With Laser Therapy in Chronic Lower Backache

Spinal Manipulation With Laser Therapy
Dry NeedlingDIAGNOSTIC_TEST

Dry Needling in Chronic Lower Backache

Dry Needling

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Those patients will be included in the study who have chronic low back pain (12 week duration).
  • both genders aged 18-60 years low back pain

You may not qualify if:

  • Those patients will be excluded in the study who have needle phobia, any infection, cancer, dermal changings, heart transplant, pregnancy, rheumatic fever(25)fracture, cauda equina syndrome, arrhythmia, sensory deficiency, mental illness, surgery, osteoporosis, low term use of steroid

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chaudary Muhammad Akram Teaching Hospital

Lahore, Punjab Province, Pakistan

RECRUITING

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Kausar Kalsoom

CONTACT

+923081841078kausarkalsoom832@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 18, 2023

First Posted

May 11, 2023

Study Start

April 1, 2023

Primary Completion

June 1, 2023

Study Completion

August 31, 2023

Last Updated

May 11, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)