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Studies were included if they (1) evaluated a yoga intervention to promote T2DM management, (2) used a comparison group, (3) reported an objective measure of glycemic control at post-intervention, and (4) had follow-up length or post-test of at least 8 weeks from baseline.
Able to follow-up participants for 2 weeks from baseline.
The Pain Coping Scenarios Questionnaire and the Pain Knowledge Questionnaire were administered at two additional time points - T2: 5 weeks from baseline and T3: 10 weeks from baseline.
Outcomes will be measured at baseline and at 6, 12, 26 and 52 weeks from baseline.
After 24 weeks on treatment (54 weeks from baseline), they were again assessed with CGIC.
All outcome measures will be assessed at baseline and at 4 and 16 weeks from baseline.
Doses were given at enrolment and repeated 4 weeks from baseline.
The LITHE Biomarker study included 585 patients followed for the first 52 weeks from baseline.
The VAS was also administered to participants at T2: 5 weeks from baseline and T3: 10 weeks from baseline to determine the impact of the intervention on pain severity, over time.
Assessments were performed at the following points of time: at baseline, at 6 weeks from baseline or at discharge if discharged before 6 weeks from baseline and at 3, 6, 12 and 24 months from baseline.
To assess physical activity, a physical performance test will be performed at 5 and 13 weeks from baseline.
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