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NCT07725471Recruiting

COMPARISON OF BREATHING AND SUBOCCIPITAL RELEASE IN STROKE

COMPARISON OF THE EFFECTS OF DEEP AND SLOW BREATHING EXERCISES AND SUBOCCIPITAL RELEASE, ADDED TO ROUTINE PHYSIOTHERAPY AND REHABILITATION, ON AUTONOMIC, MOTOR, AND COGNITIVE FUNCTIONS AND EMOTIONAL STATUS IN STROKE PATIENTS

Source: ClinicalTrials.gov · Last updated 24 Jul 2026

Brief summary (registry, in English)

The aim of this study is to investigate the positive effects of deep, slow breathing exercises and suboccipital relaxation, when added to a routine physiotherapy and rehabilitation program, on autonomic, motor, cognitive, and emotional status functions in individuals who have experienced a stroke, and to examine their superiority compared to routine physiotherapy and rehabilitation alone.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
54 (estimated)
First submitted
21 Jul 2026
Start date
6 Jul 2026
Primary completion date
1 Sept 2027
Lead sponsor
Ankara Yildirim Beyazıt University
Diseases
Stroke
NCT number
NCT07725471

What you commit to

  • Study type: Interventional
  • Planned participants: 54
  • From 6 Jul 2026 to the primary completion date, 1 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Presence of active or chronic respiratory disease
  • Low heart rate (\<60 bpm)
  • Known cardiac conduction disorder
  • Advanced liver, kidney, heart, or lung disease
  • Severe aphasia or cognitive impairment that may interfere with the informed consent process or study procedures
  • Malignant tumors or infectious diseases
  • Failure to meet the inclusion criteria

Other

  • Symptomatic carotid or vertebrobasilar stenosis
  • Severe carotid or vertebrobasilar stenosis
  • Diagnosed depression
  • Pregnancy
  • Presence of a pacemaker or other implanted electrical device
  • Spasticity of grade 4 or higher according to the Modified Ashworth Scale in the upper and lower extremities
  • Brunnstrom Motor Staging below stage 3 in the upper and lower extremities

Who the study is looking for

  • First-time diagnosis of stroke
  • Presence of unilateral hemiplegia due to ischemic or hemorrhagic stroke etiology
  • Presence of hemiparesis
  • At least 3 months post-stroke
  • Having signed the informed consent form
  • Aged between 18 and 84 years

Age in the registry: 18 years to 84 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Afyonkarahisar Health Sciences University Health Practice and Research Center
Coordinator of this site? Confirm its status
AfyonkarahisarTurkey (Türkiye)Recruiting

This page is information, not medical advice. Discuss any trial with your doctor.