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Dry needling-related objective signs of the referred pain presence

Dry needling-related objective signs of the referred pain presence based on the latent trigger point in healthy adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622001016729
Enrollment
200
Registered
2022-07-20
Start date
2024-12-01
Completion date
2025-12-31
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The aim of the study is to observe objective signs of the latent trigger points dry needling based on the distant bioelectrical muscle activity and autonomic nervous system measurement.

Interventions

The study aims to observe dry needling-related distant reactivity of the muscles and autonomic nervous system, taking into account the latent component of the trigger point form. A single assessment will be made of: (i) latent trigger point examination according to Travell& Simons diagnostic criteria and Delphy study recommendation and the measurement of the pressure pain threshold - PPT, using an AlgoMed; (ii) dry needling under infrared camera control according to the Skorupska Protocol combin

The study aims to observe dry needling-related distant reactivity of the muscles and autonomic nervous system, taking into account the latent component of the trigger point form. A single assessment will be made of: (i) latent trigger point examination according to Travell& Simons diagnostic criteria and Delphy study recommendation and the measurement of the pressure pain threshold - PPT, using an AlgoMed; (ii) dry needling under infrared camera control according to the Skorupska Protocol combine with the heart rate variability (HRV) and surface electromyography (sEMG); (iii) analysis of negative emotion and pain assessment questionnaires. A group of active athletes aged 18-35 who train in sports characterized by an asymmetric movement structure and healthy volunteers will be studied. All measurements will be performed in university laboratories. The dry needling intervention will be performed by a leading authority in the field of pain diagnosis, certified in dry needling, and who has extensive experience from international training. The intervention will include one session of 10 minutes. The intervention will be carried out by a specialist who is certified and internationally certified in the intervention to be carried out.

Sponsors

Opole University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy athletes and healthy volunteers

Exclusion criteria

- lack of informed consent to participate in the study - cardiovascular diseases, - chronic disease that impairs musculoskeletal function, - diabetes, - epilepsy, - pregnancy, - infections, - inflammatory diseases, - stroke, - oncological diseases.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 10, 2026