Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Craig et al 1996 UK | N=60 volunteer male subjects with induced DOMS affecting elbow flexor muscles. Subjects randomised into the following groups: 1. Control 2. Placebo 3. 2.5Hz Combined phototherapy/Low-intensity Laser (CLILT) 4. 5Hz CLILT 5. 20Hz CLIIT | RCT (Evidence level 2b) | 1: ROM- elbow flexion, extension and resting angles. | 1: No significant differences. | Only male subjects recruited therefore limits external validity. Limited subject inclusion and exclusion criteria stated. Did not state whether random subject allocation was concealed. Unclear if groups were comparable at baseline measures of characteristics and outcome measures. Did not state whether assessors who measured outcomes were blinded. Did not state how many subjects were included in data analysis and dropout rate not reported. Did not state point measures to quantify treatment effect or measures of variability for data obtained. |
2: Mechanical pain threshold/tenderness of 8 points of the biceps brachii. | 2: No significant differences. | ||||
3: Pain assessment using Visual analogue scale (VAS). | 3: No significant differences. | ||||
4: Pain assessment using McGill Pain Questionnaire. | 4: No significant differences. | ||||
Craig et al 1999 UK | N=36 volunteer (18 male, 18 female) subjects with induced DOMS affecting elbow flexor muscles. Subjects randomised into the following groups: 1. Control group 2.CLILT group (73Hz pulsed dose) 3.Placebo | RCT (Evidence level 2b) | 1: ROM- elbow flexion, extension and resting angles. | 1: No significant differences between groups of elbow flexion angle, elbow extension angle Elbow resting angle demonstrated significant differences between the control group, and placebo and CLILT groups; level of significance not stated and direction of differences not stated. | Limited subject inclusion and exclusion criteria stated. Did not state whether random subject allocation was concealed. Unclear if groups were comparable at baseline measures of characteristics and outcome measures. Did not state whether therapists who administered treatment were blinded. Did not state how many subjects were included in data analysis and dropout rate not reported. Did not state point measures to quantify treatment effect or measures of variability for data obtained. Graphs used to depict changes in outcome measures for all groups during experiment but no key provided therefore unable to interpret which data set belonged to each group. |
2: Mechanical pain threshold/tenderness of 8 points of the biceps brachii. | 2: No significant differences. | ||||
3: Pain assessment using VAS. | 3: No significant differences, although on day 4 subjects receiving CLILT reported a non significant increase in pain compared to control and placebo groups. | ||||
4: Pain assessment using McGill Pain Questionnaire. | 4: No significant differences between groups for McGill Pain Questionnaire scores, although on day 3 subjects receiving CLILT reported an increase in pain compared to control and placebo groups. | ||||
Parr et al 2010 USA | N=60 volunteer subjects (15 male, 15 female) with induced DOMS affecting elbow flexor muscles. Subjects randomised into the following groups: 1. 2 sessions of high powered laser (HPL) at 3 watts and 5Hz. First dose immediately after DOMS induction (4 mins duration) and second dose on day 2 (90 sec duration). 2. 1 session of HPL as above, but received sham dose on day 2. 3. Control/Placebo received sham doses on both days. | RCT (Evidence level 2b) | 1: ROM- total range of elbow ROM and elbow resting angle. | 1: No significant differences between groups for total ROM. Group 2 and 3 experienced a significant (p <.05) reduction in resting arm angle from baseline to day 2 and this returned to baseline by day 4 for both groups. Group 1 but not demonstrate reduction in resting angle on any follow up days. | Limited subject inclusion and exclusion criteria stated. Did not state whether random subject allocation was concealed. Did not state how many subjects were included in data analysis and dropout rate not reported. Therapists who administered the treatment were not blinded. |
2: Muscular point tenderness using VAS of the most tender point of the biceps brachii. | 2: No significant differences. | ||||
3: Self-reported function using QuickDASH questionnaire. | 3: No significant differences. | ||||
4: Maximal voluntary isometric force using computerised isokinetic dynamometer. | 4: No significant differences. |