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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06323941
Other study ID # UV0003
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date March 14, 2024

Study information

Verified date March 2024
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Mental practice (both in isolation and also in combination with real practice) has been shown to improve somatosensory and motor variables but so far no study has taken it into the study of women's health. Through the present study the investigators want to offer some interesting data regarding the effectiveness of mental practice combined with physical practice.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 14, 2024
Est. primary completion date March 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria: - Over 18 years of age and asymptomatic women. Exclusion Criteria: - This study will exclude those who presented a respiratory pathology, cardiac, systematic, or metabolic disease, history of recent surgery, vertebral fracture, or osteoarticular disorders of the spine area.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Motor Imagery plus therapeutic exercise
Isometric exercises (20 minutes) to which will be added a motor imagery intervention (imagining movements without actually doing them).
Therapeutic exercises
Isometric exercises (20 minutes) to which will be added a placebo motor imagery intervention (imagining a blue sky).

Locations

Country Name City State
Spain Ferran Cuenca Martínez Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Skin conductance (for asessing electrodermal activity) skin conductance is a measure of sweating which is an excitatory sympathetic monoinervative variable. pre-intervention (T0), and inmmediate post-intervention (T1) (between the first and the second measurement, about 60 minutes have elapsed because it is done on the same day)
Secondary Algometry for assessing pressure pain thresholds (Pain sensitivity) An algometer shall be used to assess pain thresholds to pressure, i.e. squeezing so that pressure is converted into pain at two points. One point in the symphysis pubis area, and one point near the tibial tuberosity pre-intervention (T0), and inmmediate post-intervention (T1) (between the first and the second measurement, about 60 minutes have elapsed because it is done on the same day)
Secondary maximal pelvic floor muscle strength (measured in grams and with the phenix device) Three measurements of maximal pelvic floor strength shall be performed with an intracavitary probe and the mean of the three measurements of maximal pelvic floor muscle strength shall be considered. pre-intervention (T0), and inmmediate post-intervention (T1) (between the first and the second measurement, about 60 minutes have elapsed because it is done on the same day)
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