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Therapeutic ExerciseNCT06073210

Mental Practice and Therapeutic Exercise in Young Nulliparous Women

A study testing Motor Imagery plus therapeutic exercise and Action observation plus therapeutic exercise in people with Therapeutic Exercise and Motor Imagery, run by University of Valencia at 1 site in Spain.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 to 30 years, women onlyHealthy volunteers can take part
What is being tested?
Motor Imagery plus therapeutic exercise and Action observation plus therapeutic exercise
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
45 participants
Where
1 siteSpain
Study dates
30 Sep 2023to 1 May 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • over 18 years of age and asymptomatic women.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Spain1 site
  • Ferran Cuenca Martínez

    Valencia, 46017

Other trials in Spain

About this study

Official title: Mental Practice and Therapeutic Exercise in Young Nulliparous Women: A Randomized Controlled Trial

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.

Being tested
Motor Imagery plus therapeutic exercise, Action observation plus therapeutic exercise, Sham action observation plus therapeutic exercise

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Motor Imagery plus therapeutic exerciseBehavioural

    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 exerciseBehavioural

    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 exerciseBehavioural

    Aerobic exercise (20 minutes) and strengthening exercise (15 minutes) to which will be added a sham action observation intervention (observing space planets).

Study groups in NCT06073210
Study groupRoleWhat they receive
Therapeutic exercise plus motor imageryExperimentalThis group will perform a therapeutic exercise programme (aerobic and strength training) to which motor imagery training will be added.
Receives: Behavioral: Motor Imagery plus therapeutic exercise
Therapeutic exercise plus action observationExperimentalThis group will perform a therapeutic exercise programme (aerobic and strength training) to which action observation training will be added.
Receives: Behavioral: Action observation plus therapeutic exercise
Therapeutic exerciseActive comparatorThis group will perform a therapeutic exercise programme (aerobic and strength training) to which sham action observation training will be added.
Receives: Behavioral: Sham action observation plus therapeutic exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pelvic Floor Muscle Strength

    maximum pelvic floor strength

    Measured: 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).

  2. Pain Pressure Threshold

    Pain sensitivity

    Measured: 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).

  3. Lumbopelvic Motor Control

    Sensorimotor control of lower limbs

    Measured: 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).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Oct 2023
  2. Study start30 Sep 2023
  3. Primary completion30 Apr 2024
  4. Study completion1 May 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06073210
Sponsor's protocol ID
UV0001
Status last verified
May 2026
First submitted
3 Oct 2023
Last updated
18 May 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Motor Imagery plus therapeutic exercise and Action observation plus therapeutic exercise in people with Therapeutic Exercise and Motor Imagery, run by University of Valencia at 1 site in Spain.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pelvic Floor Muscle Strength (time frame: 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).). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2026.

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