Table 2. Study characteristics.
Article | Control group | Experimental group | Intervention | Frequency | Assessment Post-Intervention | Follow-Up | Results |
Cleland et al.8 | n = 17 | n = 19 | Experimental: supine thoracic manipulation | One time treatment | VAS | Immediate | Manipulation: immediate reduction in pain over placebo. Experimental group averaged 15.5 mm change in VAS, placebo group averaged 4.2 mm change. |
Control: placebo thoracic manipulation | |||||||
Cleland et al.3 | None | n = 78 | Six thoracic manipulations per session via three different techniques and CROM exercise | 1–2 sessions maximum | GROC, NPRS, NDI | 2–4 days | Established six predictor variables. If patient = 4/6, post-test probability of success = 93%. If 3/6, post-test probability = 86% |
Cleland et al.14 | n = 30 | n = 30 | Thoracic manipulation vs thoracic mobilization with both groups performing CROM exercise | One time treatment | NDI, NPRS | 2–4 days | Manipulation: clinically and statistically significant reductions in disability and pain and statistically significant improvement in GROC scores. |
Cleland et al.4 | n = 70 | n = 70 | Experimental: thoracic manipulation and exercise | Experimental: two sessions of manipulation and CROM followed by three sessions of exercise | NDI, NPRS, GROC | 1 week, 4 weeks, 6 months | Manipulation: clinically significant short and long-term reduction in disability, short-term (1 week) reduction in pain and improved perceived recovery at 4 weeks and 6 months |
Control: exercise only | Control: five sessions over 4 weeks | ||||||
Fernández-de-las-Peñas et al.26 | None | n = 7 | Thoracic manipulation | One time treatment | NPRS, CROM | Immediate, 2 days | Manipulation: clinically and statistically significant decrease in pain immediately, which was sustained at 2-day follow-up. CROM: improvement in all motions but none were statistically significant at either follow-up. |
Fernández-de-las-Peñas et al.9 | n = 22 | n = 23 | Experimental: thoracic manipulation once per week (1st, 3rd, and 5th sessions)+control interventions | Five sessions over 3 weeks | VAS, CROM | Immediate | Manipulation: clinically meaningful and statistically significant reduction in pain, as well as significant improved CROM (all motions) |
Control: electrotherapy and thermotherapy program | |||||||
González-Iglesias et al.10 | n = 22 | n = 23 | Experimental: thoracic manipulation once per week for 3 weeks+control intervention | six sessions over three consecutive weeks | NPRS, CROM, NPQ | 1 week | Manipulation: statistically significant and clinically meaningful reduction in pain and statistically significant decreased disability and improved CROM (all motions) |
Control: electrotherapy, superficial thermotherapy+STM | |||||||
González-Iglesias et al.24 | n = 22 | n = 23 | Experimental: thoracic manipulation once per week (1st, 3rd, and 5th session)+control intervention | five sessions over 3 weeks | VAS, CROM, NPQ | Immediate, 2 weeks, 4 weeks | Manipulation: statistically significant and clinically meaningful decrease in pain immediately and at 2 and 4 weeks. Also statistically significant improvement in CROM and disability immediately and at 2 weeks. |
Control: electro and thermotherapy program | |||||||
Ko et al.27 | n = 26 | n = 27 | Experimental: thoracic mobilizations+control intervention | Three times per week for 6 weeks | VAS, NDI, muscular endurance of deep cranio-cervical flexors | Immediate | Mobilization: statistically significant reduction in disability and pain as well as increased cervical muscle endurance |
Control: cranio-cervical flexor exercises | |||||||
Krauss et al.17 | n = 10 | n = 22 | Experimental: thoracic manipulation | One time treatment after initial evaluation | FPS, CROM | Immediate | Manipulation: statistically significant increase in bilateral cervical rotation and statistically significant improvement in pain |
Control: no intervention | |||||||
Lau et al.20 | n = 60 | n = 60 | Experimental: thoracic manipulation+control interventions | Two times per week for eight sessions | CV angle, NPRS, NPQ, SF36Q, CROM | Immediate, 3 months, 6 months | Manipulation: statistically significant and clinically meaningful decrease in pain immediately and up to 6 months. Statistically significant improvements in disability, CV angle and CROM at all follow-ups. |
Control: infrared radiation therapy and a standard set of education materials | |||||||
Martínez-Segura et al.11 | None | Cervical n = 57; Thoracic n = 33 | Cervical: midcervical, midrange manipulation; Thoracic: AP end range upper thoracic manipulation | One time treatment | PPTs, CROM, NPRS | Immediate | Thoracic group: statistically significant and clinically meaningful decrease in pain. Improvements in PPT and CROM were shown, but were not significant. |
Puentedura et al.2 | None | Cervical n = 14; Thoracic n = 10 | Cervical: cervical manipulation; Thoracic: thoracic manipulation; | five sessions over 2 weeks | NDI, NPRS, FABQ, GROC | 1 week, 4 weeks, 6 months | Thoracic manipulation: 10% of patients met or exceeded the MDC/MCID at 4 weeks and 6 months for NDI. 40% of patients met or exceeded MDC/MCID for pain at 4 weeks whereas only 20% did so at 6 months. 20% of patients reported GROC scores equal to/greater than +5 at all follow-ups. |
Both groups: standard exercise program | |||||||
Savolainen et al.25 | None | Exercise group n = 32; Manipulation group n = 43 | Exercise group: program instructed by a PT; Manipulation group: four thoracic manipulations by a physiatrist | Exercise group: not stated; | VAS | 6 months, 12 months | Manipulation: statistically significant lower level of perceived worst pain at 12-month follow-up. Both groups demonstrated statistically significant decreases in muscular tenderness and tender thoracic levels at all follow-ups. |
Manipulation group: 1 week intervals |
Note: NDI, Neck Disability Index; NPRS, Numeric Pain Rating Scale; FABQ, Fear Avoidance Beliefs Questionnaire; FABQPA, Fear Avoidance Beliefs Questionnaire physical activity subscale; GROC, Global Rating of Change; FPS, Faces Pain Scale; CROM, Cervical Range of Motion; VAS, Visual Analog Scale; NPQ, Northwick Park Neck Disability Questionnaire; CV Angle, Craniovertebral Angle; SF36Q, SF-36 Health Questionnaire; PPTs, Pressure Pain Thresholds.