Motor Imagery Plus Therapeutic Exercise in Women With Menstrual Pain
NCT ID: NCT06674655
Last Updated: 2024-11-08
Study Results
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.
NOT_YET_RECRUITING
NA
48 participants
INTERVENTIONAL
2025-01-09
2025-09-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Exercise, Motor Imagery, and Pain Neuroscience Education for Primary Dysmenorrhea: A Randomized Trial
NCT07196150
A Research Study Exploring How Musculoskeletal Function and the Autonomic Nervous System Relate to Visceral Pain in Women With and Without Dysmenorrhea (Painful Periods).
NCT07209566
Enhancing Analgesia in Chronic Pain Through Exercise
NCT04862871
Response in Patients with Persistent Pelvic Pain to Motor Imagery Through Auditory or Visual Input. a Pilot Randomized Trial.
NCT06343649
Online Pain Neuroscience Education for Women With Primary Dysmenorrhea
NCT07237802
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.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Motor Imagery Plus Therapeutic Exercise
Motor Imagery Plus Therapeutic Exercise
This group will perform three days of lumbo-pelvic motor control exercise intervention along with a motor imagery intervention program during active breaks between exercises.
Therapeutic Exercise
Therapeutic Exercise
This group will perform a lumbo-pelvic motor control exercise program for three consecutive days.
Minimal Intervention
Minimal intervention
This group will carry out a therapeutic counseling and minimal education intervention during a one-day intervention.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Motor Imagery Plus Therapeutic Exercise
This group will perform three days of lumbo-pelvic motor control exercise intervention along with a motor imagery intervention program during active breaks between exercises.
Therapeutic Exercise
This group will perform a lumbo-pelvic motor control exercise program for three consecutive days.
Minimal intervention
This group will carry out a therapeutic counseling and minimal education intervention during a one-day intervention.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Pain intensity rated higher than 3/10 on a pain scale.
* Participants do not take pain-relief medication during the study period.
* Ages between 18 and 35 years old
Exclusion Criteria
* Any chronic pain condition unrelated to menstrual pain (e.g., fibromyalgia, chronic low back pain).
* Diagnosed gynecological conditions such as endometriosis or pelvic inflammatory disease.
* Pregnancy or breastfeeding.
* Current use of psychoactive medications that could affect pain perception.
* Any significant psychiatric condition that could interfere with study participation.
* History of recent pelvic surgery (within the last 6 months).
18 Years
35 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Valencia
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ferran Cuenca
Doctor of Physical Therapy
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Valencia
Valencia, Valènica, Spain
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Ferran Cuenca Martínez, Doctor of Physical Therapy
Role: CONTACT
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
UV0004
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.