- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07578493
Effectiveness of Dance Therapy in Stroke Patients.
May 5, 2026 updated by: Pérez-Robledo, Fátima, University of Salamanca
Effectiveness of Proprioceptive Neuromuscular Facilitation-based Dance Therapy for Patients With Chronic Stroke.
Hemiparesis following a stroke is associated with persistent deficits in postural control, balance, and social participation, especially in the chronic phase.
Dance therapy, as a multisensory intervention based on movement, music, and body expression, could promote sensorimotor integration and improve postural stability, complementing conventional physiotherapy.
The primary objective of this pilot study is to evaluate the effect of a therapeutic dance program on postural control in individuals with chronic hemiparesis.
A secondary objective is to analyze changes in functional balance and gait, as well as subjective satisfaction with the therapy.
A controlled study with two parallel groups will be conducted.
Sixteen participants with chronic hemiparesis will be recruited (n=8 experimental group; n=8 control group).
Both groups will receive standard physiotherapy, but the experimental group will also receive an 8-week therapeutic dance program, with one 30-minute session per week to complement their usual therapy.
Pre- and post-intervention assessments will be performed.
ThThe experimental group is expected to show a significantly greater improvement in posturographic and clinical parameters compared to the control group.
The results could support the implementation of dance therapy as a complementary intervention in community neurorehabilitation programs.
Study Overview
Status
Not yet recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
16
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fatima Perez-Robledo, Dr.
- Phone Number: 0034 619 885 479
- Email: fatima_pr@usal.es
Study Locations
-
-
Salamanca
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Salamanca, Salamanca, Spain, 37008
- University of Salamanca
-
Contact:
- Fatima Perez-Robledo, Dr.
- Phone Number: 0034 619 885 479
- Email: fatima_pr@usal.es
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Chronic hemiparesis (≥ 6 months post-stroke).
- Ability to maintain independent standing or with minimal assistance.
- Clinical stability to perform moderate physical exercise.
- Sufficient understanding to follow simple instructions.
Exclusion Criteria:
- Severe aphasia or other cognitive disorders that limit comprehension.
- Behavioral disorders that hinder group participation.
- Severe musculoskeletal disorders or concomitant neurological conditions.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dance therapy group
|
The experimental group will participate in an 8-week therapeutic dance program, with one 30-minute session per week, as a complement to their regular physiotherapy.
Each session will integrate: • Bilateral and diagonal PNF patterns adapted to the affected side of the body.
• Rhythmic movement guided by moderate-tempo music.
• Exercises focused on postural symmetry and weight transfer.
• Explicit and implicit motor learning strategies.
The rhythmic components will be selected to optimize audio-motor synchronization, while the PNF patterns will aim to maximize sensorimotor activation and proximal stability.
The intervention will be adaptable and progressive according to the patient's clinical response.
All participants, including those in the control group, will receive standard physiotherapy provided by their primary care center, focused on functional maintenance, mobility, and strengthening, without dance or rhythmic PNF components.
They will receive two 40-minute sessions per week, individualized and adapted to their functional status.
|
|
Active Comparator: Conventional treatment group
|
All participants, including those in the control group, will receive standard physiotherapy provided by their primary care center, focused on functional maintenance, mobility, and strengthening, without dance or rhythmic PNF components.
They will receive two 40-minute sessions per week, individualized and adapted to their functional status.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Static and dynamic postural control
Time Frame: From enrollment to the end of treatment at 8 weeks
|
The oscillation of the Center of Pressure will be recorded in millimeters during the static position (Romberg test, hold the position with feet together with eyes open and eyes closed for 52 seconds) and walking at your preferred speed.
|
From enrollment to the end of treatment at 8 weeks
|
|
Load distribution during gait
Time Frame: From enrollment to the end of treatment at 8 weeks
|
The percentage (%) of load on each leg will be recorded during walking at your preferred speed.
|
From enrollment to the end of treatment at 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction with the activity
Time Frame: After completing the 8-week intervention
|
Registration will be done using an ad hoc questionnaire with questions about interest, motivation and general satisfaction with the activity, with Likert-type response items.
|
After completing the 8-week intervention
|
|
Adherence to treatment
Time Frame: After completing the 8-week intervention
|
The percentage of sessions attended will be recorded in relation to the total number of sessions given.
|
After completing the 8-week intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
May 15, 2026
Primary Completion (Estimated)
October 30, 2026
Study Completion (Estimated)
November 30, 2026
Study Registration Dates
First Submitted
April 28, 2026
First Submitted That Met QC Criteria
May 5, 2026
First Posted (Actual)
May 11, 2026
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 5, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Stroke
- Therapeutics
- Complementary Therapies
- Exercise Movement Techniques
- Physical Therapy Modalities
- Patient Care
- Psychotherapy
- Behavioral Disciplines and Activities
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Sensory Art Therapies
- Dance Therapy
Other Study ID Numbers
- NEURODANZAUSAL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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