Health Behavior Clinical Trial
Official title:
Evaluation of a Web Application That Supports Behavior Change in Work Related Stress - a Randomized Controlled Trial
Verified date | March 2018 |
Source | Mälardalen University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A randomized controlled trial is needed to strengthen the evidence in the area of web-based
self-management programs for stress-reduction.
Aim The aim for the study is to compare the effects of the web-application that supports
behavior change in stress-management to a waiting list group in persons with perceived
stress.
Method This study will have the design of a randomized controlled trial (RCT). The CONSORT
guidelines will be used for reporting the study.
Sample: Different sectors in the region will be included. Three different high-schools in
Västerås City, social services authority in Västerås municipality, a large private company in
the region, three different clinics within the county council and the municipality of Köping
have signed the attestation of participation.
Intervention: The intervention is the program for web-based stress self-management My Stress
Control.
Procedure: After informed consent the participants will, during approximately 2-4 months by
their own go through the web-based program for stress self-management. The waiting-list group
will also get access to My Stress Control after post-measurements.
Data-analysis: Descriptive statistics will be used for demographic data. Missing data will be
replaced as recommended for the different measurements included, commonly by using the mean
for responded items within the sub scale. Inferential analyses will be conducted by using
multivariate statistical analysis.
Drop-out analysis will be conducted by comparing pre-interventions measures for those who
completed the program with those who did not.
Status | Completed |
Enrollment | 95 |
Est. completion date | December 2017 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Score 17 or more on Perceived Stress Scale -14 - Able to read and speak Swedish - Employed - Consent to take part in the study Exclusion Criteria: - Scoring 11 or more on either of sub scales of Hospital Anxiety and Depression Scale - Currently on sick leave caused by stress, anxiety or depression |
Country | Name | City | State |
---|---|---|---|
Sweden | School of Health, Care and Social Welfare; Mälardalen University | Västerås | Västmanland |
Lead Sponsor | Collaborator |
---|---|
Mälardalen University |
Sweden,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in perceive stress measured with Perceived Stress Scale -14 | Wait-list group will conduct the same measures for their corresponding "pre" and "post" measures for an estimated timeframe of 2 months. | Before intervention, at intervention completion an average of 12 weeks, and for a 3 and 6 month follow up after completed intervention | |
Secondary | Motivation for Change Questionnaire | Wait-list will complete this measure for their corresponding "pre"-measure | Before intervention. | |
Secondary | Change in self-efficacy believes for coping measured with Coping Self-Efficacy Scale | Wait-list group will conduct the same measures for their corresponding "pre" and "post" measures for an estimated timeframe of 2 months. | Before intervention, at intervention completion an average of 12 weeks, and for a 3 and 6 month follow up after completed intervention | |
Secondary | Change in perception of psychosocial factors at work measured with QPS Nordic-34+ for psychosocial factors at work | As Coping Self-Efficacy Scale | Before intervention, at intervention completion an average of 12 weeks, and for a 3 and 6 month follow up after completed intervention | |
Secondary | Change in work engagement measured with Utrecht work engagement Scale | As Coping Self-Efficacy Scale | Before intervention, at intervention completion an average of 12 weeks, and for a 3 and 6 month follow up after completed intervention | |
Secondary | Change in coping behaviors measured with Brief COPE Questionnaire | As Coping Self-Efficacy Scale | Before intervention, at intervention completion an average of 12 weeks, and for a 3 and 6 month follow up after completed intervention |
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