軟體下載點

載點一、Google play store

goo.gl/lAFzqV

載點二

http://www.gyadamall.com/alg/elec-acup.apk



ADA爽貼(ADA TENS)Product Spec.

頻率(Frequency): 1Hz20Hz

脉衝寬度(Pulse Width): 80μS

輸出電流(Rate Current): MAX80mA

額定電壓(Rate Voltage): DC 5V ±10

輸出電壓(Output Voltage): 70V~100V(±10)

環境需求: 手機USB需支援OTG功能

軟件(Software): Android OS 4.4以上



Purpose 目的

硬件+軟件可强化維繫末端消費者的連結與溝通!

携帶便利,不占空間,並以維護身體健康與現代消費者生活習慣爲出發,鎖定手機族群的依賴形成與高粘著度,亦利于傳達企業形象、産品發布的主動載具!也可在未來省下許多新品宣傳推廣的費用!陸續開發相關産品帶給客戶完美體驗,健康的維護可以是主、被動的運動,也可以是一種時尚的流行生活,讓每個人都能享受科技的樂趣!



TENS is a non-invasive, very safe method to reduce pain, both acute and chronic. While controversy exists as to its effectiveness in the treatment of chronic pain, a number of systematic reviews or meta-analyses have confirmed its effectiveness for postoperative pain, osteoarthritis, and chronic musculoskeletal pain. Conversely, results from the Bone and Joint Decade 2000 - 2010 Task Force on Neck Pain accumulated data showing no clinically significant benefit to TENS for the treatment of neck pain when compared to sham treatment. Recent clinical studies and meta-analysis suggest that using adequate intensity of stimulation is necessary to obtain analgesia with TENS.


Basic science studies show that high and low frequency TENS produce their effects by activation of opioid receptors in the central nervous system. Specifically, high frequency TENS activates delta-opioid receptors both in the spinal cord and supraspinally (in the medulla) while low frequency TENS activates mu-opioid receptors both in the spinal cord and supraspinally. Further high frequency TENS reduces excitation of central neurons that transmit nociceptive information, reduces release of excitatory neurotransmitters (glutamate) and increases the release of inhibitory neurotransmitters (GABA) in the spinal cord, and activates muscarinic receptors centrally to produce analgesia (in effect, temporarily blocking the pain gate). Low frequency TENS also releases serotonin and activates serotonin receptors in the spinal cord, releases GABA, and activates muscarinic receptors to reduce excitability of nociceptive neurons in the spinal cord.