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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06073210
Other study ID # UV0001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 30, 2023
Est. completion date April 30, 2024

Study information

Verified date October 2023
Source University of Valencia
Contact Ferran Cuenca Martinez, PhD
Phone 913456781
Email ferran.cuenca@uv.es
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 this study we want to offer some interesting data regarding the effectiveness of mental practice combined with physical practice.


Recruitment information / eligibility

Status Recruiting
Enrollment 45
Est. completion date April 30, 2024
Est. primary completion date April 30, 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
Aerobic exercise (20 minutes) and strengthening exercise (15 minutes) to which will be added a motor imagery intervention (imagining movements without actually doing them).
Action observation plus therapeutic exercise
Aerobic exercise (20 minutes) and strengthening exercise (15 minutes) to which will be added a action observation intervention (observing movements without actually doing them).
Sham action observation plus therapeutic exercise
Aerobic exercise (20 minutes) and strengthening exercise (15 minutes) to which will be added a sham action observation intervention (observing space planets).

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 Pelvic Floor Muscle Strength maximum pelvic floor strength 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).
Primary Pain Pressure Threshold Pain sensitivity 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).
Primary Lumbopelvic Motor Control Sensorimotor control of lower limbs 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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