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Status unknownNCT05680493Updated Jan 11, 2023

Comparison of Dry Needling and Manual Pressure Release for Managing Low Back Pain

An interventional study of Manual pressure release and Dry needling in Low Back Pain, sponsored by Foundation University Islamabad. Status unknown at 1 site in Pakistan. Open to participants aged 30 Years to 60 Years. Per ClinicalTrials.gov, last updated 2023-01-11.

Sponsored by Foundation University Islamabad · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2022), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

This study will compare the effect of dry needling and manual pressure in patients having low back pain in terms of pain and disability. There will be two groups ; experimental and control. Half of study group will receive dry needling session along with hot pack. Half of study group will receive manual pressure technique along with hot pack.

Read the detailed description

The study is Randomized Control Trail , which is being conducted in fauji foundation hospital and Foundation University College Of Rehabilitation (oct 2022-feb 2023) . Sample size of 50 individual was calculated using epitool with 95% confidence interval (CI), and power 80%. sample will be collected through pilot study .

both groups will recieve conventional physiotherapy protocol (hot pack) Assessment will be done on baseline, and 4th week .

02

Conditions studied

  • Low Back Pain
03

In context

Back Pain

2,373 studies on the registry are indexed under Back Pain; 284 are open to participants now.

This study's planned enrollment of 30 is below the median of 60 across 1,941 interventional studies indexed under Back Pain.

Browse Back Pain studies →

Lead sponsor

Foundation University Islamabad is the lead sponsor of 238 studies on the registry; 128 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:-

  • age between 30-60
  • pateint with subacute and chronic low back pain at least last 6 months.
  • pateint with active MTrps.

Exclusion Criteria:

  • patient with fibromyalgia
  • pregnant females
  • patient with chronic diseases (osteoporosis, lungs disease and diabetes)
  • patient with musculoskeletal injuries
  • patient that are using any medication to relief pain like analgesic or muscle relaxants
  • Any treatment for back pain in same period of research.
  • patient having any radiculopathies or discogenic low back pain
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Dry needling

    Total 12 sessions of trigger point dry needling at lumbar muscles with Hot pack,with 3 sessions per week

    Procedure: Dry needling · Procedure: Heat therapy

  • Active comparator
    manual pressure release

    Hot pack for 15 min then manual pressure release

    Procedure: Manual pressure release · Procedure: Heat therapy

Interventions

  • ProcedureManual pressure release

    lengthens the muscle up to the increasing resistance, then gradually applies gentle pressure on MTrp until fingers feels a definite increase in tissue resistance (first barrier). Pressure would maintain until clinician sense relief of tension

  • ProcedureDry needling

    A filiform needle is inserted at 45 degree in to trigger point and then twirl the needle up and down to release trigger point

  • ProcedureHeat therapy

    Hydro collator pack will be placed on affected area for relaxation and pain relief for 15 min

06

What researchers measure

Primary outcomes

  1. pain intensity

    visual analogue scale

    Time frame: 4 weeks

  2. functional disability

    functional disability will be measured through oswestry disability index

    Time frame: 4 weeks

07

Study locations

1 site
  • Foundation University College of Physical Therapy
    Rawalpindi, Punjab 46000, Pakistan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 11, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05680493
Lead sponsor
Foundation University Islamabad
Responsible party
Sponsor
First posted
Jan 11, 2023
Start date
Oct 1, 2022
Primary completion
Jan 1, 2023 (estimated)
Completion
Feb 1, 2023 (estimated)
Last update
Jan 11, 2023

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2022. You cannot join it, but the record below documents what was studied.

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