Examining of the Acute Effects of Low-Level Laser Therapy (LLLT) on Pain Threshold and Tolerance: a Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 62
- 试验地点
- 1
- 主要终点
- Electrical Pain Threshold Intensity (mA)
研究概览
简要总结
Pain is defined by the International Association for the Study of Pain as "an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage." Low-Level Laser Therapy (LLLT) has gained attention as a safe, noninvasive intervention with analgesic and anti-inflammatory effects. This study examines whether a single session of LLLT can produce immediate changes in pain threshold and pain tolerance in healthy adults, compared to a sham laser control.
详细描述
Pain is defined by the International Association for the Study of Pain as "an unpleasant sensory and emotional experience associated with, or resembling that associated with, actual or potential tissue damage." Pain can be classified into several types: nociceptive pain, neuropathic pain, and nociplastic pain. Nociceptive pain results from actual or potential damage to non-neural tissue and is due to the activation of nociceptors. It is typically acute and arises from injury, inflammation, or mechanical stimuli. Neuropathic pain is caused by damage or disease affecting the somatosensory nervous system. Nociplastic pain involves altered nociception despite no clear evidence of tissue damage or nerve injury.
Acute nociceptive pain is one of the most common presentations in musculoskeletal conditions and plays a crucial protective role by alerting the body to tissue damage and prompting healing responses. However, when inadequately controlled, it may induce central sensitisation and predispose patients to chronic pain syndromes. To address acute pain non-pharmacologically, physiotherapists typically employ a multimodal approach, including Transcutaneous Electrical Nerve Stimulation (TENS), which harnesses sensory-level stimulation to activate spinal inhibitory circuits and dampen pain signals; therapeutic ultrasound (US), where mechanical vibration and mild thermal effects accelerate inflammatory resolution and collagen synthesis; cryotherapy and thermotherapy, which modulate local tissue temperature to reduce nociceptor excitability and optimize perfusion; and manual therapy, including joint mobilization, soft tissue techniques, and muscle energy methods, that elicit both mechanical and neurophysiological analgesia, improving range of motion and function.
More recently, laser therapy has emerged as a powerful adjunct for acute pain relief. Laser therapy refers to the medical use of specific light wavelengths to elicit therapeutic effects in tissues. Broadly, there are two main types used in physiotherapy: High-Intensity Laser Therapy (HILT) and Low-Level Laser Therapy (LLLT). HILT operates at higher power outputs and can penetrate deeper tissues, producing photothermal effects. In contrast, LLLT, also termed photobiomodulation or cold laser therapy, uses lower power levels and longer exposure times, primarily inducing photochemical and photobiological changes without significant heating. LLLT is favoured for its safety and gentle stimulation of tissue repair across a wide range of conditions.
LLLT involves the application of red or near-infrared light, typically between 600 and 1100 nm, at low intensities to avoid thermal effects. It has been widely adopted in clinical practice due to its non-invasive nature, minimal side effects, and effectiveness in reducing pain, promoting wound healing, and modulating inflammation.
The mechanisms underlying LLLT are thought to involve the absorption of photons by cellular chromophores, particularly cytochrome c oxidase in the mitochondria. This enhances mitochondrial respiration and ATP production, modulates reactive oxygen species, and induces transcription factors that promote cell survival and tissue repair. These effects may also extend to modulation of the autonomic nervous system, where LLLT has been shown to promote parasympathetic activity and reduce sympathetic dominance, contributing to analgesic and anti-inflammatory outcomes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Single (Participant)
盲法说明
Participants blinded to group assignment. Researcher administering intervention unblinded; participants wear safety glasses in both groups to maintain blinding.
入排标准
- 年龄范围
- 18 Years 至 35 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Age between 18 and 35 years
- •Healthy individuals without chronic medical conditions
- •Free from chronic or acute pain
- •All genders
- •Able to provide informed consent
排除标准
- •Menstruation at the time of testing
- •Sensory deficits (failure to pass sharp-dull test)
- •Pregnancy
- •History of epilepsy
- •Presence of cardiovascular conditions (including pacemaker)
- •Acute hand injuries
- •Diagnosed neurological disorders
- •Use of analgesics or NSAIDs within the previous 48 hours
- •Contraindications to low-level laser therapy or electrical stimulation (e.g., light sensitivity, malignancy)
研究组 & 干预措施
Low-Level Laser Therapy (LLLT)
Participants in this group will receive active Low-Level Laser Therapy (LLLT) using a 904 nm wavelength Chattanooga model 422 laser device at 1000 Hz. The laser will be applied for 2 minutes per point to three standardized points over the medial epicondyle region (total of 6 minutes). The energy dose is 0.9 J/cm². All participants and the researcher will wear appropriate laser safety eyewear.
干预措施: Low-Level Laser Therapy (LLLT) (Device)
Sham LLLT
Participants in this group will undergo the same procedure, positioning, device placement, application duration, and safety eyewear use as the active LLLT group; however, the laser device will be deactivated. No therapeutic light energy will be delivered. This sham procedure is used to control for placebo and expectation effects.
干预措施: Sham LLLT (Other)
结局指标
主要结局
Electrical Pain Threshold Intensity (mA)
时间窗: Pre-intervention and immediately post-intervention
Electrical pain threshold will be measured using tetanic faradic stimulation with gradual increases in current intensity. The cathode will be placed on the palmar surface of the third finger and the anode over the medial epicondyle. Participants will verbally indicate the point at which the electrical sensation is first perceived as painful. The stimulation intensity (in milliamperes) at this point will be recorded.
Electrical Pain Tolerance Intensity (mA)
时间窗: Pre-intervention and immediately post-intervention
Electrical pain tolerance will be measured using tetanic faradic stimulation using the same electrode placement and stimulation parameters. Participants will verbally indicate the maximum level of pain they are willing to tolerate. The stimulation intensity (in milliamperes) at this point will be recorded.
次要结局
未报告次要终点
研究者
Yara Mabrouk Ibrahim Mabrouk Houtar
Physiotherapist
European University of Lefke
