Alexander 2015.
Study characteristics | ||
Methods |
Study design: randomised controlled trial Study grouping: parallel group |
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Participants |
Baseline characteristics Yoga
Control (No intervention)
Overall
Included criteria: no prior experience with yoga, willingness to complete eight weekly sessions and homework exercises, and willingness to be randomly assigned to the research or control group. Excluded criteria: serious illness or major orthopaedic diagnoses of the neck, back, pelvis, or lower extremities that could interfere with completion of the yoga intervention protocol. Pretreatment: NR Compliance rate: NR Response rate: NR Type of healthcare worker: exclusively nurses |
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Interventions |
Intervention characteristics Yoga
Control (no intervention)
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Outcomes | MBI
Health Promoting Lifestyle Profile II (HPLP II)
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Identification |
Sponsorship source: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This research was supported by the Research and Creative Activities Fund of Texas Christian University. Country: USA Setting: Hospital Comments: NR Authors name: Gina K. Alexander Institution: Texas Christian University, Harris College of Nursing and Health Sciences Email: g.alexander@tcu.edu Address: TCU Box 298620, Fort Worth, TX 76129, USA Time period: NR |
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Notes | MBI‐EE included in analysis 2.1 | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Questionnaire, and core study questionnaires. After individuals completed consent forms and baseline assessments, they were enroled in the study and randomized to the intervention (yoga) or usual care control group. A total of 54 individuals Sequence generation process not mentioned |
Allocation concealment (selection bias) | Unclear risk | Insufficient information to understand whether intervention allocations could have been foreseen in advance of, during, enrolment. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Participants were not blinded. |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Participants were not blinded whereas outcomes are self‐reported |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Not reported. |
Selective reporting (reporting bias) | Unclear risk | No trial registration or study protocol reported in the study and we did not find one online. No indication of selective reporting. |
Other bias | Unclear risk | Compliance rate and response rate not reported. |