Motor Imagery and Isometric Exercises on Pelvic Floor Sensorimotor Condition

NCT ID: NCT06323941

Last Updated: 2024-03-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-01

Study Completion Date

2024-03-14

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Isometric Exercise Motor Imagery Women's Health

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Motor Imagery plus Isometric Exercise

This group will perform a therapeutic exercise programme (isometric exercises training) to which motor imagery training will be added.

Group Type EXPERIMENTAL

Motor Imagery plus therapeutic exercise

Intervention Type BEHAVIORAL

Isometric exercises (20 minutes) to which will be added a motor imagery intervention (imagining movements without actually doing them).

Isometric Exercise

This group will perform a therapeutic exercise programme (isometric exercises training) to which sham motor imagery training will be added.

Group Type ACTIVE_COMPARATOR

Therapeutic exercises

Intervention Type BEHAVIORAL

Isometric exercises (20 minutes) to which will be added a placebo motor imagery intervention (imagining a blue sky).

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Motor Imagery plus therapeutic exercise

Isometric exercises (20 minutes) to which will be added a motor imagery intervention (imagining movements without actually doing them).

Intervention Type BEHAVIORAL

Therapeutic exercises

Isometric exercises (20 minutes) to which will be added a placebo motor imagery intervention (imagining a blue sky).

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Valencia

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ferran Cuenca

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ferran Cuenca Martínez

Valencia, , Spain

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Spain

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

UV0003

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Interoception and Body Scan
NCT06237530 COMPLETED PHASE1/PHASE2