This study is designed as a randomized controlled intervention with a pre-test-post-test design to evaluate the effect of reflexology on pain, physiological parameters, and sleep quality in stroke patients. The study will be conducted at the Physical Therapy and Rehabilitation Unit of Van Training and Research Hospital between October 2024 and June 2025.

Using a simple randomization method, patients will be assigned to either the control group or the reflexology intervention group, with an anticipated sample size of 35 patients per group. Data will be collected using the Personal Information Form, the Visual Analog Scale (VAS), the Richards-Campbell Sleep Scale (RCSS), and a physiological parameters recording form.

Patients in the intervention group will receive reflexology massage twice a week for six weeks, for a total of 12 sessions. Each session will last 30 minutes (15 minutes per foot), in addition to routine nursing care. Physiological parameters will be recorded before and after each reflexology session. The control group will receive routine nursing care only, and their physiological parameters will be monitored twice weekly using the same schedule. All scales and forms will be administered again at the end of the 6-week period.

The study aims to determine whether reflexology influences pain levels, physiological parameters, and sleep quality in stroke patients. Findings from this research may contribute to the evidence base regarding complementary interventions in post-stroke nursing care; however, no study results are yet available in this protocol record.

This study is designed as a randomized controlled experimental trial to evaluate the effects of reflexology applied to individuals who have experienced a stroke on pain levels, physiological parameters, and sleep quality. The study includes an intervention group and a control group and aims to examine the role of reflexology within a holistic nursing care approach.

The research will be conducted between October 2024 and June 2025 at the Physical Therapy and Rehabilitation Unit of Van Training and Research Hospital. A single-blind method will be used, in which information about group assignment will be concealed from participants. Ethical committee approval has been obtained from a foundation university, and institutional approval has been received from the hospital where the study will take place.

Using a simple randomization method, patients will be assigned to either the reflexology group or the control group, with an anticipated sample size of 35 participants in each group. Data will be collected using the Personal Information Form, the Visual Analog Scale (VAS), the Richards-Campbell Sleep Scale (RCSS), and a physiological parameters recording form.

Participants in the intervention group will receive reflexology massage twice a week for six weeks, for a total of 12 sessions, each lasting 30 minutes (15 minutes per foot), in addition to routine nursing care. Physiological parameters will be recorded before and after each reflexology session. Participants in the control group will receive routine nursing care only, and their physiological parameters will be monitored twice weekly following the same schedule. All forms and scales will be administered again at the end of the sixth week.

This study aims to determine whether reflexology has an effect on pain, physiological parameters, and sleep quality in individuals who have experienced a stroke. The findings of the study will contribute to the evidence base regarding complementary practices used in nursing care; however, no study results are reported in this protocol record.

Inclusion Criteria:

Individuals over the age of 18,

• No diagnosis of any psychiatric illness or medication use,
• Hemiplegic stroke patients,
• Volunteering to participate in the study,
• According to the patient introduction form; patients describing hemiplegic shoulder pain and insomnia symptoms,
• No history of neurological or psychiatric disorders other than stroke,
• No irritation or ulceration in the skin area where reflexology will be performed,
• No history of deep vein thrombosis,
• Able to speak and understand Turkish and able to read and write,
• Patients who voluntarily agree to participate in the study will be included.

Exclusion Criteria:

Refusal to participate in the study,

• Tetraplegic and paraplegic patients,
• Patients with stroke due to malignant brain damage undergoing chemotherapy or radiotherapy
• Those with mental and psychiatric disorders,
• Those who have received professional massage therapy within the past month,
• Those with contraindications for foot massage and reflexology: patients with generalized edema, pacemakers, history of heart attack, active gout, history of deep vein thrombosis, history of gallbladder and kidney stones, acute infection, fever, fractures, or wounds will not be included in the study.

individual participant data will be shared with other researchers. Data will be anonymized to protect participant privacy, and access will be provided upon request under specified conditions.

Individual participant data will be made available beginning 6 months after study completion and will remain accessible for a period of 5 years.

Access to the de-identified individual participant data will be granted to qualified researchers who provide a methodologically sound research proposal and obtain ethics committee approval. Requests must include a brief study plan and justification for the use of the data. Data will be shared through secure institutional channels upon approval by the principal investigator and the hosting institution.