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Motivational intervention as a booster kinesitherapeutic standard treatment in hospitalized depressed patients Effects on the effectiveness and sustainability

Motivational intervention as a booster kinesitherapeutic standard treatment in hospitalized depressed patients Effects on the effectiveness and sustainability

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009800
Enrollment
76
Registered
2016-04-06
Start date
2016-07-04
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

F32 F33 F34

Interventions

Group 1: The intervention group in addition to the standard treatment of kinesitherapeutic LVR Clinic Cologne offered to participate in a short educational and motivational intervention, including a w

Sponsors

LVR-Klinik Köln Akademisches Lehrkrankenhaus der Universität zu Köln
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 63 Years

Inclusion criteria

Inclusion criteria: Indication for participation in the study is a diagnosis of "depressive disorder" according to ICD-10 (F32.x Depressive Episode, F33.x Recurrent depressive disorder and F34.x Persistent affective disorder), regardless of severity, diagnosed by the doctor on the respective station (only patients of the Division I and II) and regardless of whether a single or a recurrent episode is present. A further condition is a value from the BDI greater 18th.

Exclusion criteria

Exclusion criteria: Exclusion criteria are Orthopaedic, neurological or cardiovascular problems that preclude physical stress and make the processing of the test methods employed impossible. Furthermore, patients are excluded with acute psychotic symptoms from study participation.

Design outcomes

Primary

MeasureTime frame
The primary target variables: the habitual physical activity is defined as the primary endpoint. We expect that these more highly correlated with the depression as the objective parameters. Questionnaire habitual physical activity (PCA) by Wagner & Singer, 2003: The questionnaire is to all 3 Measurement times (t0 enrollment, t1 after 4 weeks, t2 two months after completion of hospitalization) applied.

Secondary

MeasureTime frame
Secondary outcome variables: The secondary target variables are the physiological parameters of aerobic endurance and general physical fitness, depressive symptoms, HRQL and the quality of attention. - Test: 2 Km Walking Test after Bos, 2001 and Motor basic diagnostic (MBK) to Wydra, 2000: - Questionnaire: Beck Depression Inventory Audit (BDI-II) after Wintjen & Petermann, 2010: - Questionnaire: Short Form Health Questionnaire (SF-36) according to Bullinger & Kirchberger 1998: - Questionnaire: Mindful Attention Awareness Scale (MAAS) by Brown and Ryan 2003: All tests and questionnaires to all 3 Measurement times (t0 enrollment, t1 after 4 weeks, t2 two months after completion of hospitalization) applied.

Countries

Germany

Contacts

Public ContactFrank Sauer

LVR-Klinik Köln

frank.sauer@lvr.de0221-8993232

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026