Braining - Physical Exercise in Psychiatry - Evaluation of Feasibility, Implementation and Health Among Staff

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRegion Stockholm

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

80 Participants
are grouped into 2 trial groups
Group A: Unit A
Group B: Unit B

Trial outcomes

Primary outcomes

1

Minutes spent on Physical movement (high, moderate, low)

Physical exercise conducted by staff, measured by actigraph

Time frame
Change from baseline to follow up observation 6 months after inclusion
2

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)

Time frame
Change from baseline to follow up observation 6 months after inclusion
3

General health

General health measured by self ratings of General health questionnaire (GHQ), scores 0-12, higher scores indicates more mental distress

Time frame
Change from baseline to follow up observation 6 months after inclusion
4

Perceived stress

Perceived stress measured by self ratings of Perceived stress scale (PSS-10), , scores 0-40, higher scores indicates more mental distress

Time frame
Change from baseline to follow up observation 6 months after inclusion

Secondary outcomes

1

Burnout

Burnout measured by self ratings of Burnout Shirom-Melamed Burnout Questionnaire (SMBQ-6), scores 6-42, higher scores indicates more burnout symptoms

Time frame
Change from baseline to follow up observation 6 months after inclusion
2

Burnout

Burnout measured by self ratings of Burnout Shirom-Melamed Burnout Questionnaire (SMBQ-6), scores 6-42, higher scores indicates more burnout symptoms

Time frame
Follow up 12 months after inclusion
3

Sleep difficulties

Sleep difficulties measured by self ratings of Insomnia Severity Index (ISI), , scores 0-28, higher scores indicates more sleep difficulties

Time frame
Change from baseline to follow up observation 6 months after inclusion
4

Sleep difficulties

Sleep difficulties measured by self ratings of Insomnia Severity Index (ISI), , scores 0-28, higher scores indicates more sleep difficulties

Time frame
Follow up 12 months after inclusion

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Region Stockholm

Lead sponsor

Karolinska Institutet

Collaborator