NCT04548323

Brief Summary

The main objective is to identify the hypoalgesic effect of the imagination of actions in sedentary subjects with high levels of physical activity.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Sep 2020

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 7, 2020

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 14, 2020

Completed
16 days until next milestone

Study Start

First participant enrolled

September 30, 2020

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2020

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2021

Completed
Last Updated

September 14, 2020

Status Verified

September 1, 2020

Enrollment Period

3 months

First QC Date

September 7, 2020

Last Update Submit

September 7, 2020

Conditions

Keywords

Motor imagery

Outcome Measures

Primary Outcomes (6)

  • Pain pressure threshold

    Pressure 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

    Change from baseline and immediately post-intervention

  • Temporal sumation

    Temporal summation is a somatosensory measure that is performed by making small punctures in the area of interest.

    Change from baseline and immediately post-intervention

  • Electrodermal activity

    Electrodermal 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

    Change from baseline and immediately post-intervention

  • Respiration Rate

    Respiration Rate will be measured through a pressure transducer located in the centre of the chest, where it was fixed by a strap.

    Change from baseline and immediately post-intervention

  • Heart rate

    Heart Rate will be measured by three electrodes located in the left area of the chest. One of the electrodes was placed in the middle zone while a second electrode was positioned on the lateral side, and a third one on the lower left side, below the first electrode.

    Change from baseline and immediately post-intervention.

  • Salivary stress

    The Salivary Stress Test is a study that assesses fatigue and the type of stress (acute, moderate or chronic) presented by the subject.

    Change from baseline and immediately post-intervention.

Secondary Outcomes (2)

  • Visual and Kinesthetic Motor Imagery Ability

    Change from baseline and immediately post-intervention

  • The degree of physical activity

    Immediately before the intervention.

Study Arms (2)

Motor Imagery in Sedentary subjects

Behavioral: Motor imagery

Motor Imagery active subjects

Behavioral: Motor imagery

Interventions

Motor imageryBEHAVIORAL

Subjects will perform motor imagery tasks on the motor gestures of running and walking.

Motor Imagery active subjectsMotor Imagery in Sedentary subjects

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Healthy subjects divided by their physical activity levels.

You may qualify if:

  • asymptomatic participants
  • men and women aged 18 to 65 years

You may not qualify if:

  • insomnia
  • nausea
  • headache
  • pregnancy
  • use of painkillers in the last 24 hours
  • presence of metal inside the head
  • pacemaker
  • wound on the area of electrodes' application
  • drug consumption; (j) recent application of tDCS
  • psychiatric disease impeding understanding of the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CSEU La Salle

Madrid, 28023, Spain

Location

MeSH Terms

Conditions

Agnosia

Condition Hierarchy (Ancestors)

Perceptual DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Roy A La Tocuhe, physiotherapist PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 7, 2020

First Posted

September 14, 2020

Study Start

September 30, 2020

Primary Completion

December 30, 2020

Study Completion

July 30, 2021

Last Updated

September 14, 2020

Record last verified: 2020-09

Locations