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Completed

NCT Number: NCT07746596

SU JOK FOR DYSPNEA AND FATIGUE

As the disease progresses, dyspnea and fatigue may increasingly interfere with daily activities, reduce patients' independence, and negatively affect their quality of life. Therefore, in addition to pharmacological treatment, there is a need for safe and supportive interventions to help alleviate these symptoms. This study aims to evaluate the effects of Su Jok therapy on dyspnea and fatigue in patients with chronic obstructive pulmonary disease (COPD). The findings are expected to provide evidence regarding the potential role of Su Jok therapy as a complementary intervention for symptom management. The results may contribute to improving patients' symptom control and quality of life while providing healthcare professionals with evidence to support clinical decision-making and nursing care.

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Key information

About this study

Chronic obstructive pulmonary disease (COPD) is a progressive respiratory disease characterized by persistent airflow limitation and symptoms such as dyspnea and fatigue, which substantially impair patients' functional capacity and quality of life. Although pharmacological treatment is the cornerstone of COPD management, complementary non-pharmacological interventions may provide additional benefits in symptom control.

Su Jok therapy is a complementary therapy based on the stimulation of corresponding points on the hands and feet. It has been proposed as a simple, non-invasive, and low-cost intervention that may help reduce symptom severity and improve patient well-being. However, evidence regarding its effectiveness in patients with COPD is limited.

This study is designed as a randomized controlled trial to evaluate the effects of Su Jok therapy on dyspnea and fatigue in patients with COPD. Eligible participants will be randomly assigned to either an intervention group receiving Su Jok therapy in addition to routine care or a control group receiving routine care alone. Dyspnea and fatigue will be assessed using validated measurement instruments before and after the intervention. The primary objective is to determine whether Su Jok therapy provides additional benefits in reducing dyspnea and fatigue compared with routine care alone. The findings are expected to contribute to the evidence base regarding complementary therapies in COPD management and to support evidence-based nursing practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Adults aged 18 years or older. Diagnosed with chronic obstructive pulmonary disease (COPD). Able to communicate verbally. Expected to remain hospitalized for at least 5 days to ensure completion of the intervention.

No major health condition other than COPD that could adversely affect activities of daily living (e.g., open wounds, cancer, or gastrointestinal disorders).

Provided written informed consent to participate in the study. A Visual Analog Scale (VAS) score of 3 or higher for dyspnea and fatigue

Exclusion criteria

Patients who do not provide written informed consent to participate in the study.

Patients who are unable to communicate verbally. Patients with conditions that would prevent the application of Su Jok therapy to the hands, such as neuropathy, amputation, open wounds, or other hand disorders.

Treatment and study plan

su jok therapy

Other

Su Jok therapy was administered by the researcher once daily for five consecutive days in addition to routine COPD care. The intervention involved stimulation of predefined Su Jok correspondence points on the hands according to the study protocol. Each session was performed using standardized procedures to ensure consistency throughout the study.

Primary outcomes

  1. Dyspnea

    Time frame: Baseline and daily for 5 consecutive days, with post-intervention assessment on Day 5.

    Dyspnea severity will be assessed using the Visual Analog Scale (VAS). Higher scores indicate greater dyspnea severity.

Secondary outcomes

  1. fatigue severity

    Time frame: Baseline and post-intervention (Day 5).

    fatigue severity will be assessed using the Visual Analog Scale (VAS) and the fatıgue Severity Index (ISI). Higher scores indicate greater fatıgue severity.

Sponsors and collaborators

Lead sponsor

Erzincan Binali Yildirim Universitesi

Other

Registry information

Official study title

EFFECTS OF SU JOK THERAPY ON DYSPNEA AND FATIGUE IN PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE: A RANDOMIZED CONTROLLED TRIAL

Acronym: SUJOK-COPD

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Aug 5, 2026
Registry last updated
Aug 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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