Strain-Counterstrain Treatment of Piriformis Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorLoma Linda University

About this trial

The purpose of this investigator-initiated study is to provide an efficient and non-invasive treatment option for pain caused by the piriformis muscle.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

18 to 65 years of age

Tender point (or trigger point) in piriformis muscle determined by physical exam

Disqualifiers

Less than 45 degrees of active hip flexion, less than 5 degrees of active hip internal rotation or less than 30 degrees of active hip external rotation, on side of affected piriformis

Unable to lay prone

Non-English speaker

Inability to attend 2 sessions within the same month

Trial design

Design model

Parallel

Treatments tested in this trial

  • Strain-Counterstrain treatment of piriformis muscle

    Other intervention

    Participant will lay prone on table with affected leg close to edge of table. Piriformis muscle tender point is identified and palpated. Then patient leg is passively moved off table and passive hip flexion, abduction, and possible internal/external rotation is added to reduce tender point by 70% or more. This is done passively. This position is held for 90 seconds and then participant is passively returned back to neutral prone position with leg on table. Tender point is palpated again to reassess for change in pain (using subjective visual analog scale). An algometer is also used pre and post to assess objective change in pressure pain threshold.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Piriformis Strain-CounterstrainExperimental treatment 1 intervention
Group B: Hamstring Strain-CounterstrainSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Algometer - Change in pressure pain threshold

Objective improvement in pressure/pain threshold

Time frame
Pre and post each treatment. There are 2 treatments, 1-2 weeks apart from one another.

Secondary outcomes

1

Change in Visual Analog Scale

Subjective improvement in low back/leg pain

Time frame
Pre and post each treatment. There are 2 treatments, 1-2 weeks apart from one another.
2

Change in Oswestry Disability Index

Assesses pain with doing different activities (sleeping, walking, sitting, etc), assesses ability to do activities of daily living

Time frame
Before first treatment and after second treatment. Each treatment is 1-2 weeks apart (anticipated).

Other outcomes

Sponsors and contacts

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