Foundation University College of Physical Therapy
Islamabad, Punjab Province, 44000, Pakistan
Location status: Recruiting
NCT Number: NCT07838584
This randomized controlled trial aims to compare the clinical effectiveness of ischemic release and sustained pressure direct myofascial release for upper trapezius trigger points.
The study will compare their effects on pain pressure threshold, cervical range of motion, and scapular upward rotation following a two-week intervention.
Interested in participating?
Request Info18 year–35 year
All sexes
Interventional
Not applicable
Islamabad, Punjab Province, 44000, Pakistan
Location status: Recruiting
Eligible participants will be recruited through purposive sampling. Upper trapezius trigger points will be assessed by manual palpation to identify a taut band and hypersensitive nodule, followed by pressure to determine reproduction of the participant's familiar pain. Baseline assessments will include pain pressure threshold, cervical range of motion, and scapular upward rotation. After baseline assessment, 42 participants will be allocated randomly into respective groups, each having 21 participants.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive a two-week physiotherapy program with three sessions per week. Each session will include heat application followed active ROM and passive stretching.
Participants in Group A will receive ischemic compression in addition to standard physiotherapy. Pressure should be applied via thumb for 20 second - 1 minute until pain decreases or muscle begin to relax.
Other names: Ischemic compression
Participants will receive a two-week physiotherapy program with three sessions per week. Each session will include heat application followed active ROM and passive stretching. Participants in Group B will receive sustained pressure direct MFR in addition to standard physiotherapy. Apply pressure to the trigger point for 8-20 seconds, maintaining it until a physical "discharge" or release is felt, which may take five minutes or more.
Time frame: Baseline and after 2 weeks.
Pain pressure threshold will be assessed using a Wagner digital algometer.
Time frame: Baseline and after 2 weeks
Cervical ROM will be assessed using a goniometer.
Time frame: Baseline and after 2 weeks
Scapular upward rotation will be assessed using a bubble inclinometer.
Contact information is provided by the study sponsor or research team.
Quratulain Saeed, MS-OMPT
CONTACT
Sohaima Javed, DPT
CONTACT
Foundation University Islamabad
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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