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NCT Number: NCT07538310

Laser Acupuncture for Fatigue in Hemodialysis Patients

The goal of this clinical trial is to learn if laser acupuncture (low-level laser therapy) works to treat fatigue and improve quality of life in adults with end-stage renal disease (ESRD) undergoing hemodialysis. It will also learn about how laser acupuncture affects blood circulation and autonomic nervous system balance.

The main questions it aims to answer are:

1. Does laser acupuncture reduce the severity of fatigue and its interference with daily life? 2. Can laser acupuncture improve related symptoms such as insomnia, poor appetite, and skin itching? 3. How does laser acupuncture affect objective markers like microcirculation and heart rate variability? Researchers will compare laser acupuncture to a sham treatment (a look-alike procedure using a device that does not emit a laser) to see if laser acupuncture works to treat fatigue.

Participants will:

1. Receive laser acupuncture or a sham treatment during their regular hemodialysis sessions 3 times a week for 4 weeks. 2. Have their fatigue and life quality assessed through questionnaires on the first day, at 4 weeks, and at 8 weeks. 3. Undergo non-invasive tests to measure microcirculation, heart rate variability, and pulse waves, and have photos of their tongue taken for Chinese medicine assessment.

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Key information

About this study

Scientific Rationale Fatigue is a prevalent and debilitating symptom in patients with end-stage renal disease (ESRD) undergoing maintenance hemodialysis (HD). It is a multidimensional condition influenced by anemia, uremia, and the long-term psychosocial stress of dialysis. Conventional pharmacological treatments often yield limited efficacy for fatigue and sleep disturbances while posing risks of adverse effects. Non-pharmacological interventions, such as acupressure and exercise, have shown potential, but high-quality clinical evidence remains insufficient. Laser acupuncture (LA), or photobiomodulation (PBM), is a non-invasive, non-thermal therapy that applies low-level laser energy to traditional acupuncture points. It is proposed to modulate mitochondrial function, reduce oxidative stress, and inhibit inflammatory responses, offering a safe alternative for patients who may not be suitable for or are fearful of traditional needle acupuncture.

Study Protocol and Intervention This is a randomized, double-blind, sham-controlled pilot trial. A total of 50 participants will be recruited from the hemodialysis center and randomly assigned to either the experimental (LA) group or the sham control group in a 1:1 ratio.

  • Experimental Group: Participants will receive low-level laser therapy at specific acupoints: KI1 (Yongquan), ST36 (Zusanli), SP10 (Xuehai), PC8 (Laogong), EX-UE9 (Bafeng), EX-UE9 (Baxie), and LU9 (Taiyuan). Each session lasts 15-30 minutes, administered 3 times per week during the dialysis process for a duration of 4 weeks.
  • Sham Control Group: Participants will undergo an identical procedure using a sham device that mimics the operation and appearance of the laser equipment but does not emit actual laser energy, ensuring the maintenance of blinding.

Technical Assessment and Data Analysis

To objectively evaluate the systemic effects of LA on the circulatory and autonomic nervous systems, this study integrates several biomedical engineering technologies:

  • Microcirculation Analysis: Skin microvascular blood flow and blood volume changes are monitored using Laser Doppler Flowmetry (LDF) and Photoplethysmography (PPG).
  • Vascular and Autonomic Assessment: Brachial Pulse Wave (BPW) analysis will be used to evaluate arterial stiffness, while Heart Rate Variability (HRV) will assess the balance of the sympathetic and parasympathetic nervous systems.
  • Traditional Chinese Medicine (TCM) Evaluation: Standardized tongue diagnosis photography and the Constitution in Chinese Medicine Questionnaire (CCMQ) will be used to track changes in the participants' TCM constitutional types and internal "Qi" and blood status.

Statistical analysis will utilize t-tests or Mann-Whitney U tests to compare symptom improvement between groups. Mixed-effects models or Generalized Estimating Equations (GEE) will be employed to evaluate the long-term impact of treatment on blood pressure and microcirculation while controlling for potential confounding factors such as age and dialysis vintage.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with End-Stage Renal Disease (ESRD) who require regular maintenance hemodialysis.
  • Must undergo hemodialysis treatment at least 3 times per week.
  • Aged 18 years or older.
  • Willing and able to provide informed consent to participate in the study.

Exclusion criteria

  • Presence of acute infectious symptoms.
  • Unstable vital signs.
  • Diagnosis of malignant tumors.
  • Pregnancy.
  • Presence of open wounds at the sites designated for laser intervention.
  • Patients with implanted cardiac pacemakers or other cardiac devices.

Treatment and study plan

Low-Level Laser Acupuncture (LA)

Device

Device: Low-level laser therapy (LLLT) device. Acupoints: KI1 (Yongquan), ST36 (Zusanli), SP10 (Xuehai), PC8 (Laogong), EX-UE9 (Bafeng), EX-UE9 (Baxie), and LU9 (Taiyuan).

Dosage/Frequency: Administered 3 times per week during the hemodialysis process for 4 weeks.

Duration: Each treatment session lasts approximately 15 to 30 minutes.

Sham laser acupuncture

Device

Description:Device: An inactive sham laser device that is identical in appearance and operational procedure to the active device.

Procedure: The device will be applied to the same 7 acupoints (KI1, ST36, SP10, PC8, Bafeng, Baxie, LU9) for 15-30 minutes.

Blinding: The device will not emit actual laser energy but will mimic the treatment process to maintain participant blinding.

Frequency: 3 times per week for 4 weeks during hemodialysis.

Primary outcomes

  1. VAS for fatigue

    Time frame: Baseline (Day 0), Week 4 (end of intervention), and Week 8 (follow-up).

    The VAS is a subjectively reported scale used to evaluate fatigue intensity. Participants mark their fatigue level on a 100-mm line ranging from "no symptoms" (0) to "most severe symptoms" (100). Higher scores indicate more severe fatigue.

  2. Brief Fatigue Inventory (BFI)

    Time frame: Baseline (Day 0), Week 4 (end of intervention), and Week 8 (follow-up).

    The BFI consists of 9 items assessing the severity of fatigue and its impact on daily functional activities over the past week. Each item is scored from 0 to 10, with higher total scores representing more severe fatigue and greater interference with daily life.

Secondary outcomes

  1. Kidney Disease Quality of Life 36 (KDQOL-36)

    Time frame: Baseline, Week 4, and Week 8.

    Kidney Disease Quality of Life (KDQOL). A specific instrument to assess the quality of life in patients with kidney disease. The scores range from 0 to 100, where higher scores represent a better quality of life (better health status).

  2. Laser Doppler Flowmetry Analysis (LDFA) Score

    Time frame: Baseline, Week 4, and Week 8.

    Integrate multiple features from the Laser Doppler Flowmetry (LDF) thermal hyperemia process, including the amplitudes of various peaks and the total area under the curve, into a single continuous variable score via a specific computational model. This score is utilized to evaluate the overall physiological status of the microcirculation. Since the score is a continuous variable, it does not have a predefined minimum or maximum limit. Higher numerical values indicate higher peripheral blood flow velocity and better microvascular function.

  3. Photoplethysmography Analysis (PPGA) Score

    Time frame: Baseline, Week 4, and Week 8.

    A composite score derived from PPG signals. The PPG waveform is captured through photoelectric conversion and processed using Fast Fourier Transform (FFT) to obtain the frequency domain spectrum. Specific spectral features are extracted and integrated based on the Harmonic Series Principle to calculate the final PPGA score.

    Since the score is a continuous variable based on spectral energy distribution, it does not have a predefined maximum limit. Higher numerical values indicate a pulse pattern more consistent with healthy physiological status.

  4. Brachial Pulse Wave Analysis (BPWA) score

    Time frame: Baseline, Week 4, and Week 8.

    A composite score derived from the Brachial Pulse Wave (BPW) to assess the hemodynamic characteristics and arterial stiffness of the upper limb. The brachial pressure waveform is captured and processed using Fast Fourier Transform (FFT) to obtain the frequency domain spectrum. Specific spectral features are extracted and integrated based on the Harmonic Series Principle to calculate the final BPWA score.

    Since the score is a continuous variable based on spectral energy distribution, it does not have a predefined minimum or maximum limit. Higher numerical values indicate a pulse pattern more consistent with healthy arterial elasticity and physiological status.

  5. Heart Rate Variability (HRV)

    Time frame: Baseline, Week 4, and Week 8.

    Analysis of time variations between heartbeats to assess the balance between sympathetic and parasympathetic nervous systems and overall stress status.

  6. Constitution in Chinese Medicine Questionnaire (CCMQ)

    Time frame: Baseline, Week 4, and Week 8.

    Constitution in Chinese Medicine Questionnaire (CCMQ). This scale assesses the individual's TCM constitution. Each subscale score ranges from 0 to 100. For the "Gentle" (Neutral) constitution, higher scores indicate a healthier state. For the other eight "Biased" constitutions (e.g., Yang-deficiency, Qi-stasis), higher scores indicate a more severe imbalance or worse condition.

  7. Tongue Moisture Index (TMI)

    Time frame: Baseline, Week 4, and Week 8.

    An assessment of tongue moisture using an Artificial Intelligence (AI) image recognition system. The AI model analyzes digital tongue images to extract hydration-related features and classifies or scores the degree of moisture. The score ranges from 0 to 100, where a higher score indicates a higher level of tongue hydration (more moisture).

Study contacts

Contact information is provided by the study sponsor or research team.

Chao-Tsung Chen, Ph.D.

CONTACT

[email protected]

+886-979-306-080

Ming Jen Wang, MD

CONTACT

[email protected]

+886-930-766-631

Sponsors and collaborators

Lead sponsor

Taipei City Hospital

Other Gov

Collaborators

  • National Taiwan University of Science and Technology
  • National Yang Ming Chiao Tung University

Registry information

Official study title

Laser Acupuncture Improves Fatigue and Quality of Life in Hemodialysis Patients: a Randomized Double-blind Clinical Trial Pilot Study

Acronym: LA-HD-Fatigue

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Apr 20, 2026
Registry last updated
Apr 20, 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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