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Acute Effects of Action Observation on Neck Pain

Acute Effects of Action Observation on Pain Intensity, Muscle Strength, Tactile Acuity and Pressure Pain Threshold.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05078489
Enrollment
60
Registered
2021-10-14
Start date
2021-11-20
Completion date
2023-02-15
Last updated
2023-02-21

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

Conditions

Neck Pain

Brief summary

This study aims to assess the immediate effects of action observation therapy on the cervical muscles' strength, pain intensity, tactile acuity and pain pressure threshold in individuals with chronic nonspecific neck pain.

Detailed description

This study is a randomized controlled trial with two arms: action observation group vs control group. The action observation group will be asked to watch videos of neck exercises with full attention and concentration and not perform any motion or execute any movement during the observation time. The control group will be asked to watch videos of a landscape. Participants will be assessed at baseline and at post-intervention for muscle strength, pain intensity, pressure pain threshold and tactile acuity.

Interventions

OTHERAction-observation therapy

Action observation therapy involves the observation and perception of human movement performed by others. The observation of actions performed by others activates in the perceiver the same neural structures responsible for the actual execution of those same actions.

OTHERPlacebo

Participants will watch a natural landscape without any human.

Sponsors

Aveiro University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Have nonspecific chronic neck pain, defined as a recurrent or persistent pain that lasts more than 3 months, with no trauma or etiology/diagnosis associated.

Exclusion criteria

* Visual and hearing dysfunction not corrected by eyeglasses/contact lenses or a hearing aid; * Infectious diseases; * Cervical myelopathy; * Cervical surgery; * Cervical fracture or/and subluxation; * Vestibular pathology; * Neurological disorder/deficits; * Rheumatic autoimmune diseases; * History of cancer; * Severe cervical trauma.

Design outcomes

Primary

MeasureTime frameDescription
Pressure pain thresholdsBaselinePressure pain thresholds are the minimum amount of pressure applied with an algometer that is perceived as being painful; is measured in Kgf

Secondary

MeasureTime frameDescription
Pain intensityBaselineMeasured with a 100 mm Visual Analogue Scale
Neck flexors strengthBaselineA dynamometer will be used against the forehead of the participants to quantify the isometric strength and units of measurement will be Newtons.
Tactile acuityBaselineAssessed as the ability of the participant to distinguish two points using a caliper and the measurement units is millimetres.
Neck extensors strengthBaselineA dynamometer will be used against the posterior part of the head of the participants to quantify the isometric strength and units of measurement will be Newtons.
Neck lateral flexors strengthBaselineA dynamometer will be used against the lateral aspect of the head of the participants to quantify the isometric strength and units of measurement will be Newtons.

Other

MeasureTime frameDescription
Fear of movementBaselineMeasured with the TAMPA Scale of Kinesiophobia (range: 13-52 and higher values are indicative of higher levels of fear of movement)
Fear-avoidance beliefsBaselineMeasured with the Fear-Avoidance Beliefs Questionnaire (range: 0-66 with higher scores indicating higher fear-avoidance beliefs)
DisabilityBaselineMeasured using the Neck Disability Index (Range: 0 - 50 and higher values indicate higher disability)
CatastrophizingBaselineMeasured with the Catastrophizing Scale (range 0-52 and higher values are indicative of higher pain catastrophizing)

Countries

Portugal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026