Effects of Dry Needling Using Spinal and Peripheral Sites Versus Peripheral Sites Only

NACompletedINTERVENTIONAL
Enrollment

34

Participants

Timeline

Start Date

October 27, 2017

Primary Completion Date

May 1, 2019

Study Completion Date

May 1, 2019

Conditions
Plantar FasciitisAchilles TendinitisPatellofemoral Pain Syndrome
Interventions
PROCEDURE

Spinal and Peripheral Dry Needling

Participants will be positioned lying flat and the relevant spinal level will be treated using a Seirin L- type 50 mm needle. The needle will be inserted to a depth no greater than three-quarters length of the needle for 30 seconds using a vertical pistoning technique and then statically up to 10 minutes.

PROCEDURE

Peripheral Dry Needling

Participants will be positioned lying flat and the relevant peripheral points will be treated using a Seirin L- type 50 mm needle. The peripheral treatment site(s) will be determined by the physical therapist's palpation of active or latent trigger points or tender points. The needle will be inserted to a depth no greater than three-quarters length of the needle for 30 seconds using a vertical pistoning technique and then statically up to 10 minutes.

Trial Locations (1)

30322

The Emory Clinic, Atlanta

All Listed Sponsors
lead

Emory University

OTHER

NCT02646579 - Effects of Dry Needling Using Spinal and Peripheral Sites Versus Peripheral Sites Only | Biotech Hunter | Biotech Hunter