F32 F33
Conditions
Interventions
Group 1: Individual training (6 weeks, 1 session per week, individual training, modules endurance, strength, flexibility, coordination, relaxation, participants choose individual activity, offer of ta
Sponsors
Medizinische Hochschule Hannover
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: moderate to severe depressive illness (F32, F33), written consent, residence near study cite
Exclusion criteria
Exclusion criteria: no capacity to consent, acute substance abuse, acute suicidality, other relevant diseases interfering with measurements (e.g. pacemaker), pregnancy or lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| moderate to vigorous physical activity (min/day) 12 weeks after intervention (measurement with accelerometer GT9X Link (ActiGraph, Pensacola, Florida, USA) and analysis with software ActiLife 6 (ActiGraph, Pensacola, Florida, USA)) | — |
Secondary
| Measure | Time frame |
|---|---|
| activity (Freiburger Fragebogen zur körperlichen Aktivität), quality of life (World Health Organization Quality of Life-Bref), severity of depressive symptoms (Montgomery Asberg Depression Scale, Beck-Depressions-Inventar II), physical performance (6 Minute walking distance, stair climb, star excursion balance test, Sit-to-stand test, grip strength, Chair Sit-and-reach-test ), body composition (bioelectrical impedance analysis (InBody 720, JP Global Markets GmbH, Eschborn, Germany), waist-to-hip-ratio, bodyweight, height), level of functioning/disability (WHO Disability Assessment Schedule 2.0), working ability (days of incapacity to work), motivation (Behavioural Regulation in Exercise Questionnaire-3), dietary habits (Mediterranean Diet Adherence Screener, questionnaire) and costs | — |
Countries
Germany
Contacts
Public ContactKatriona Keller-Varady
Medizinische Hochschule Hannover
Outcome results
None listed