About this trial
Physical exercise (PE) shows beneficial effects on somatic and psychiatric symptoms. "Braining" is a clinical invention where psychiatric staff exercise together with patients to help patients start and execute PE regularly. In the present study feasibility of the intervention will be evaluated, how Braining is perceived and implemented, and effects on health and physical activity among staff. It is hypothesized that staff health and physical activity will increase after implementing Braining at the unit. Braining will be implemented at four psychiatric units in Region Stockholm, Sweden. During 6 months staff will be trained and receive implementation support. To measure feasibility the staff will answer self-rating questionnaires and be invited to a focus group interview post the implementation period. Implementation will be evaluated by ratings of compliance, the self-rating questionnaire Normalization Process Theory Measure (S-NoMAD), and focus group interviews. Health will be measured by self ratings of stress, sleep, general health, and engagement pre implementation and every month during the 6 month implementation phase. Ratings will be repeated at follow up 12 month after implementation started. Physical activity will be rated during the 6 months implementation phase using a tracker of activity and at follow up 12 month after implementation started. All staff at the units will be invited to participate in the evaluations, approximately 20 individuals per unit.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Works at one of the relevant units regardless of occupational category, including administrative services.
Permanent employment or fixed-term employment for at least one more year after the start of studies.
Disqualifiers
Medical conditions such as heart or lung disease, infection, abstinence where heart rate-increasing physical activity is considered contraindicated due to Medical reasons.
Full-time sick leave> 1 month during the training period
Trial population
Staff of a psychiatric care unit
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Minutes spent on Physical movement (high, moderate, low)
Physical exercise conducted by staff, measured by actigraph
Minutes spent on Physical movement self rated (high, moderate, low)
Physical exercise conducted by staff, measured by self ratings of International Physical Activity Questionnaires (IPAQ)
General health
General health measured by self ratings of General health questionnaire (GHQ), scores 0-12, higher scores indicates more mental distress
Perceived stress
Perceived stress measured by self ratings of Perceived stress scale (PSS-10), , scores 0-40, higher scores indicates more mental distress
Secondary outcomes
Burnout
Burnout measured by self ratings of Burnout Shirom-Melamed Burnout Questionnaire (SMBQ-6), scores 6-42, higher scores indicates more burnout symptoms
Burnout
Burnout measured by self ratings of Burnout Shirom-Melamed Burnout Questionnaire (SMBQ-6), scores 6-42, higher scores indicates more burnout symptoms
Sleep difficulties
Sleep difficulties measured by self ratings of Insomnia Severity Index (ISI), , scores 0-28, higher scores indicates more sleep difficulties
Sleep difficulties
Sleep difficulties measured by self ratings of Insomnia Severity Index (ISI), , scores 0-28, higher scores indicates more sleep difficulties
Sponsors and contacts
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Region Stockholm
Lead sponsor
Karolinska Institutet
Collaborator