The Use of Combined Motor Imagery and Action Observation to Evaluate the Influence on Functional Parameters Such as Strength, Range of Motion, Pain or Fear of Movement Among Others, in Females Breast Cancer Survivors.

NCT07067710 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2025-07-16

No results posted yet for this study

Summary

The aim of this study is to evaluate the effectivity of the combined motor imagery and action observation therapies to improve functional parameters such as strenght, range of motion, pain or fear of movements among others in relation to upper limb in breast cancer survivors. The main question it aims to answer is: Will a combined therapy of motor imagery and action observation improve the strenght, rang of motion, pain, limb diameter and fear of movement of the upper limb in breast cancer survivor females? The participants will be part of the IM-OA23 proyect that consist on seeing some diferent videos about upper limb mobility and then they'll have to imagine the movements and to performed themselves. Researches will compare two groups (control group and intervention group) to evaluate the diferences between them.

Conditions

  • Breast Cancer Survivor

Interventions

OTHER

Motor imagery combined with action observation

To observe and imaging one action with a video resource. Not virtual reality.

Sponsors & Collaborators

  • Instituto de Investigación Sanitaria de Navarra (IdiSNA)

    collaborator UNKNOWN
  • Fundacion Miguel Servet

    lead OTHER

Principal Investigators

  • Paula Escalada-Hernández, PhD · Public University of Navarra

  • Nelia Soto-Ruiz, PhD · Universidad Pública de Navarra

  • Pilar Arnal-Vallés, Candidate PhD · Hospital of Navarra

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-25
Primary Completion
2025-04-28
Completion
2026-02-28

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07067710 on ClinicalTrials.gov