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Dry Needling and Patients Treatment Expectations

Influence of Induced Expectations on the Autonomic Nervous System During a Dry Needling Intervention for Patients With Neck Pain. A Randomized Clinical Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04636879
Enrollment
45
Registered
2020-11-19
Start date
2021-02-23
Completion date
2026-11-05
Last updated
2026-05-01

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

Conditions

Neck Pain; Dry Needling; Motivation

Brief summary

Objectives The aim of this study is to compare the effects of inducing positive expectations against negative or neutral induced expectations on the activation of the Autonomic Nervous System and the analgesic response, after a dry needling technique in upper trapezius fibers in patients with unspecific neck pain. Summary Theoretical framework: Dry needling has proven its efficacy for the treatment of myofascial trigger points. Moreover, it has proven its effects over the Central Nervous System and the Autonomic Nervous System (ANS). Despite that previous studies have researched the role of patient's expectations and their relationship with the results of treatment, there is insufficient information concerning the effects of inducing expectations and the activation of the ANS during the application of widely used therapies, such as dry needling.

Detailed description

The aim of this study will be to research the effects of induced expectations combined with a dry needling technique on the activation of the ANS and on the results of the treatment. Hypothesis: The induction of a positive expectation shall cause a greater analgesic response associated with a response in the ANS compared to the induction of neutral or negative expectations. Methods: Patients with neck pain will participated in this randomized clinical trial, which will be randomly assigned into 3 groups in order to receive positive, neutral or negative expectations concerning the treatment, by means of an individual informative talk. All subjects will received treatment using dry needling in the upper trapezius fibers. The main variables measured will be the following: Analogic Visual Scale, Pressure Pain Threshold using a mechanical Force Gage (before and after) and the activation of the ANS measuring the skin conductance, skin temperature, heart rate and breathing rate (monitored for 5 minutes before the intervention, during and 20 minutes afterwards).

Interventions

OTHERPositive expectation AND dry needling in the upper trapezius fibers, at the most painful point

The subjects will received the same treatment, using dry needling in the upper trapezius fibers, at the most painful point after receiving the corresponding message.

OTHERNeutral expectation AND dry needling in the upper trapezius fibers, at the most painful point

The subjects will received the same treatment, using dry needling in the upper trapezius fibers, at the most painful point after receiving the corresponding

OTHERNegative expectation AND dry needling in the upper trapezius fibers, at the most painful point

The subjects will received the same treatment, using dry needling in the upper trapezius fibers, at the most painful point after receiving the corresponding

Sponsors

University of Alcala
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Neck pain. * Hiperalgesic point in Upper trapezius muscle.

Exclusion criteria

* Pain Irradiation toward upper limb * Psychological disorders * Whiplash. * Neuropathic symptoms * Cervical and / or Shoulder Spine Surgery

Design outcomes

Primary

MeasureTime frameDescription
Skin conductance (µS).Change from baseline at twenty minutesIt is the measure of the variations in the electrical resistance of the skin, caused by the excitation of the sweat glands, controlled by the Sympathetic Nervous System (SNS)

Secondary

MeasureTime frameDescription
Heart rate variabilityChange from baseline at twenty minutesThis variable is defined as the variation of the heartbeat in a previously defined period in an analysis of consecutive circadian periods. It measures the time in milliseconds between the R waves of two consecutive beats (known as the RR interval) and is widely used in the field of Cardiology for the stratification of patients after an acute myocardial infarction. It has also been shown to be a useful tool in detecting ANS activation.
Pain intensityChange from baseline at twenty minutesIt will be collected through the Visual Analogue Scale (VAS). It is a continuous scale, which consists of a 100 mm horizontal straight line, so that zero is equivalent to "total absence of pain" and 100 to "more bearable pain.
Pressure pain thresholdChange from baseline at twenty minutes.The pressure pain threshold is defined as the minimum amount of pressure necessary to cause pain. It has been measured through a Force Dial FDK using a mechanical Force Gage (Wagner Instruments).

Countries

Spain

Contacts

CONTACTDaniel Pecos-Martín, PhD
daniel.pecos@uah.es+ 34 918855142
CONTACTDaniel Somkereki, Master
clinica.fisio@fgua.es636869373
STUDY_CHAIRDaniel Pecos-Martin, PhD

Alcala University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 2, 2026