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Effect-evaluation of the intervention “Being active without Worries”.

Effect-evaluation of the intervention “Being active without Worries”, an intervention aimed at reducing depressive and stress symptomatology in adult low- SES women from disfavourized communities.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20588
Enrollment
240
Registered
2005-08-26
Start date
2005-08-30
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

1. B-condition, the eight- week intervention is offered with only the exercise component
2. BP-condition, the eight- week intervention is offered with the exercise and psycho- education components
3. A C-condition, a control condition with postponed intervention for 3 months. (see also summary for explanation).

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: The research population consists of adult women (20-55 yrs) with a low- SES background. Furthermore, the women must have mild to moderate (sub clinical) depressive symptomatology as measured with the CES- D, or suffer from stress related complaints.

Exclusion criteria

Exclusion criteria: Because of the design of the intervention, participants are not allowed to have severe hearing problems or severe physical handicaps.

Design outcomes

Primary

MeasureTime frame
Depressive and stress related symptomatology, as measured by the CES-D, perceived stress scale, daily hassles scale. These measures will be administered two weeks before subjects start the course, 1 week after ending the course and next 6, 12 and 18 months after ending the course.

Secondary

MeasureTime frame
Secondary outcomes are social support, mastery, self- esteem, self- efficacy, assertiveness and neighborhood perception These will be measured two weeks before subjects start the course, 1 week after ending the course and next 6, 12 and 18 months after ending the course by means of questionnaires as the SSL, personal mastery scale, the NPV, ALCOS and the SIG. Percentage of participating women will be determined by means of enrollment numbers for the course, satisfaction with the course will be determined by means of a questionnaire.

Contacts

Public ContactJudith Waerden, van der

University Maastricht (UM), Department of Health Education and Promotion, P.O. Box 616

+31 (0)43 388 2131

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)