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Action Observation and Motor Imagery Induced Hypoalgesia in Asymptomatic Subjects

Action Observation and Motor Imagery Induced Hypoalgesia in Asymptomatic Subjects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03959449
Enrollment
30
Registered
2019-05-22
Start date
2019-06-05
Completion date
2019-07-15
Last updated
2019-07-23

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

Conditions

Analgesia, Exercise

Keywords

Motor imagery, Action observation, Hypoalgesia

Brief summary

This study evaluates the influence of motor imagery and the observation of actions on pain perception. Participants in this study are asymptomatic subjects who will perform an IM and AO protocol of an aerobic exercise.

Detailed description

Motor Imagery (MI) is defined as a dynamic mental process that involves the representation of an action, in an internal way, without its actual motor execution. The Action Observation (AO) evokes an internal, real-time motor simulation of the movements that the observer is perceiving visually. Both mental processes trigger the activation of the neurocognitive mechanisms that underlie the planning and execution of voluntary movements in a manner that resembles how the action is performed in a real manner. The phenomenon of exercise-induced hypoalgesia is well known. This is why it has been suggested that these techniques could produce pain modulation similar to that produced by real exercise.

Interventions

Action observation (video) and motor imagery of running.

BEHAVIORALMotor imagery

Motor imagery of running

BEHAVIORALExercise plus action Observation and motor imagery

Real exercise of running during 6 min plus action observation (video) and motor imagery of running.

Sponsors

Universidad Autonoma de Madrid
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 18 and 60 * Healthy and with no pain subjects

Exclusion criteria

* Any cognitive impairment that hindered viewing of audiovisual material. * Difficulty understanding or communicating. * Presence of systemic pathology, Central Nervous System or rheumatic disease. * Inadequate understanding of the Spanish language to follow instructions for measuring and treatment. * Collaboration of pregnant women. * Underage subjects * Subjects with pain at the time of the study.

Design outcomes

Primary

MeasureTime frameDescription
Pain pressure thresholdChange from baseline and immediately post-interventionPressure Pain Threshold (PPT) is one of these tests and it is defined as the minimum force applied which induces pain. The measurement shall be carried out by using an algometer (pressure device that induces mechanical stimuli) is to standardize the amount of pressure applied in the neck region. The reliability of pressure pain thresholds according to raters or measurement frequencies is relatively high

Secondary

MeasureTime frameDescription
Visual and Kinesthetic Motor Imagery AbilityImmediately before the interventionVisual and Kinesthetic Motor Imagery Ability will be measured with Movement Imagery Questionnaire-Revised (MIQ-R). MIQ-R has four movements repeated in two subscales, a visual and a kinesthetic one. Additionally, a score between 1 and 7 is assigned, with 1 representing difficulty in picturing the motor image or difficulty in feeling the movement previously made, and 7 representing the maximum ease. The internal consistencies of the MIQ-R have been consistently adequate with Cronbach's α coefficients ranging above 0.84 for the total scale, 0.80 for de visual subscale and 0.84 for the kinesthetic subscale (Campos & González, 2010).
The degree of physical activityImmediately before the interventionThe degree of physical activity was objectified through the The International Physical Activity Questionnaire (IPAQ) questionnaire, which allows the subjects to be divided into three groups according to their level of activity, which can be high, moderate, and low or inactive. The IPAQ consists of 7 questions about the frequency, duration and intensity of activity (moderate and intense) performed in the last seven days, as well as walking and sitting time on a workday. The IPAQ scoring protocol assigns the following MET values to walking, moderate, and vigorous intensity activity: 3.3 METs, 4.0 METs, and 8.0 METs, respectively.
KinesiophobiaImmediately before the interventionFear of movement or kinesiophobia will be quantified with the Spanish version of the Kinesiophobia Tampa Scale (TSK-11). This instrument demonstrates reliability and validity in patients with chronic pain, being shorter than the original scale. The total score ranges from 11 to 44 points, with the highest scores indicating greater fear of a new injury due to movement
Electrodermal ActivityChange in electrodermal activity after 5 minutes post-interventionElectrodermal Activity will be measured through the use of two electrodes that recorded changes in conductance through the skin located at the back of the dominant hand
Respiration RateChange in electrodermal activity after 5 minutes post-interventionRespiration Rate will be measured through a pressure transducer located in the centre of the chest, where it was fixed by a strap

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026