Table 1.
Study | Size | Design | Duration | Intervention | Controls | Outcomes | AEs |
---|---|---|---|---|---|---|---|
Eng et al. (2006) [17] | |||||||
USA | 25 | Open-label | 6 months | 24 sessions of acupuncture with Tui Na massage and Qi Gong | – |
Motor: 2.4 points worsening on mUPDRS from baseline Non-motor: 16% improvement on PDQ-39 (p = 0.044) and 29% improvement on BDI (p = 0.006) Qualitative: 3 reported no change, 4 mild, 9 moderate, and 7 marked improvement |
Safe and well tolerated |
Doo et al. (2015) [16] | |||||||
Korea | 11 | Open-label | 12 weeks | 24 acupuncture + BVA sessions | – |
Motor: UPDRS parts II and III improved significantly from baseline (5-point improvement) Improved gait speed (2-s improvement) Non-motor: PDQL improved significantly from baseline (122 to 147) |
Some reported slight bleeding or pain; some redness or itchiness with BVA. No serious adverse effects |
Fukuda et al. (2015) [19] | |||||||
Japan | 27 | Open-label | 1 visit | 1 acupuncture session | – | Motor: improvement in gait speed (60.4 to 66.2 m/min, p = < 0.001), step length (53.7 to 57.7 cm, p = < 0.001), floor reaction force (0.26 to 0.29 m/s2, p = < 0.001), and cadence (112.7 to 114.8 steps/min, p = 0.007) | Did not report |
Shulman et al. (2002) [18] | |||||||
USA | 20 | Open-label | 5 weeks or 8 weeks | Twice weekly acupuncture sessions | – |
Motor: no improvement in mUPDRS or other quantitative motor assessments Non-motor: on SIP, only significant improvement in sleep and rest category (p = 0.03); no change in total score; no improvement in BDI or BAI Qualitative: 85% of patients reported subjective improvement of symptoms including tremor, walking, handwriting, slowness, pain, sleep, depression, and anxiety |
Safe and well tolerated |
Yu et al. (2019) [20] | |||||||
Taiwan | 15 | Controlled trial, groups assigned based on patient preference | 8 weeks | Twice weekly acupuncture sessions (n = 9) | Usual care, with oral pain medications only (n = 7) |
Motor: improvement in total UPDRS (− 21.6%, p = 0.005), but not motor subscale Non-motor: KPPS improved from baseline (− 46.2%, p = 0.023); no change in BDI, PDSS-2, and PDQ-39 |
|
Ren (2008) [21] | |||||||
China | 80 | Randomized, controlled | Unspecified | 2 courses of 10 sessions of acupuncture (n = 50) given every 3–5 days | Levodopa (Madopar) only (n = 30) | Motor: significantly lower dose of Madopar in the treatment group after intervention (752 mg vs 504 mg, p < 0.05) | Did not report |
Aroxa et al. (2017) [22] | |||||||
Brazil | 22 | Randomized, controlled | 8 weeks | Weekly acupuncture sessions (n = 11) | Usual care (n = 11) | Non-motor: PDSS showed significant improvement from baseline in sleep quality, nocturnal psychosis, and nocturnal motor symptoms compared to baseline; no difference between groups | Did not report |
Cristian et al. (2005) [23] | |||||||
USA | 14 | Randomized, controlled, double-blind | 2 weeks | 5 EA sessions (n = 7) | EA in non-acupuncture sites (n = 7) |
Motor: non-significant trend toward improvement in mUPDRS Non-motor: non-significant trend toward improvement on PDQ-39 ADL subscale and summary index; no change in GDS Qualitative: subjective improvements in nausea and sleep |
Did not report |
Cho et al. (2012) [24] | |||||||
Korea | 43 | Randomized, controlled, double-blind | 8 weeks | Twice weekly BVA (n = 14) or regular acupuncture sessions (n = 15) | Usual care (n = 14) |
Motor: Both interventions had improvement in mUPDRS from baseline; BBS and 30-m walking time improved in BVA from baseline; total UPDRS and mUPDRS improved relative to controls in BVA Non-motor: BDI improved from baseline in the regular acupuncture group |
One patient reported itchiness with BVA. No serious adverse events |
Toosizadeh et al. (2015) [25]; Lei et al. (2016) [26] | |||||||
USA | 15 | Randomized, sham-controlled, double-blind | 3 weeks | Weekly EA sessions (n = 10) | Sham acupuncture at placebo sites (n = 5) |
Motor: Compared to baseline, the EA group had improved balance based on measures of sway and significant improvement in mUPDRS, specifically falls and rigidity (67% and 48%, respectively; p = 0.02); significant improvement in UPDRS II and III and rigidity subscale compared to controls (p < 0.05) In specific measures of gait and balance, significant improvement from baseline in speed, stride length, and mid-swing speed; improvement compared to controls in most measures of gait, especially speed (effect size 0.32–1.16, p = 0.001) |
One patient with transient lightheadedness during procedure No serious adverse events |
Kluger et al. (2016) [27] | |||||||
USA | 94 | Randomized, sham-controlled, double-blind | 6 weeks | Twice weekly acupuncture sessions (n = 47) | Sham acupuncture with toothpicks at placebo sites (n = 47) |
Motor: no improvement in mUPDRS in either group after 6 weeks Non-motor: no between-group differences on the MFIS, though both groups improved significantly from baseline at 6 weeks and 12 weeks |
One patient reported constipation that resolved after stopping acupuncture |
Cho et al. (2018) [28] | |||||||
Korea | 73 | Randomized, sham-controlled, double-blind | 12 weeks | Twice weekly BVA sessions (n = 29) | Sham acupuncture with normal saline (n = 29), usual care (n = 15) |
Motor: Compared to usual care, the BVA group had improvement in UPDRS II and III and PIGD, but not compared to sham acupuncture; both BVA and sham improved significantly from baseline on mUPDRS, 20-m step at 12 weeks, but only BVA had sustained improvements at 20 weeks Non-motor: PDQL improved in both groups at 12 weeks, sustained only in the BVA group at 20 weeks, BDI was improved in the BVA group at 20 weeks |
Some patients reported mild pain or slight bleeding after acupuncture and mild itchiness or swelling after BVA No serious adverse events |
Kong et al. (2018) [29] | |||||||
Singapore | 40 | Randomized, sham-controlled, double-blind | 5 weeks | Twice weekly acupuncture sessions (n = 20) | Sham acupuncture with retractable needles (n = 20) |
Motor: significant improvement from baseline on mUPDRS in the acupuncture group, but not compared to controls Non-motor: Both groups had significant improvement from baseline on the MFI, but no between-group differences; no improvement from baseline on PDQ-39, GDS, and ESS |
2 serious adverse events from falls, not felt to be related to acupuncture; 1 worsening of anxiety |
AEs = adverse events; BAI = Beck Anxiety Inventory; BBS = Berg Balance Scale; BDI = Beck Depression Inventory; BVA = Bee Venom Acupuncture; EA = electroacupuncture; ESS = Epworth Sleepiness Scale; GDS = Geriatric Depression Scale; KPPS = King’s Parkinson’s Disease Pain Scale; MFI = Multidimensional Fatigue Inventory; MFIS = Modified Fatigue Impact Scale; mUPDRS = Unified Parkinson’s Disease Rating Scale, motor subscale; PDQ-39 = 39-item Parkinson’s Disease Questionnaire; PDQL = Parkinson’s Disease Quality of Life Questionnaire; PDSS = Parkinson’s Disease Sleep Scale; PDSS-2 = Parkinson’s Disease Sleep Scale 2; PIGD = Postural Instability and Gait Disturbance score; SIP = Sickness Impact Profile; UPDRS = Unified Parkinson’s Disease Rating Scale