Skip to content

Exercise treatment for depression: a randomized, controlled study of a computeranimated endurance sport in a virtual setting – Effects on depression, self-efficacy, acceptability and feasibility

Exercise treatment for depression: a randomized, controlled study of a computeranimated endurance sport in a virtual setting – Effects on depression, self-efficacy, acceptability and feasibility - AVATAR Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00004882
Enrollment
40
Registered
2013-07-25
Start date
2013-07-08
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

F32 F33

Interventions

Group 1: The exercise group participates daily for ten days in a computer-animated endurance sport for 20 minutes with cardiopulmonary exercise. Group 2: The placebo group carries out stretching exerc

Sponsors

Schlosspark-Klinik Abt. Psychiatrie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Major depression according to the ICD-10 (single or recurrent episode ; F32, F33), confirmed by the Standardized Diagnostic Interview for Mental Disorders, „Mini-DIPS“ 2. HAMD-17 score of at least 15 3. Participants have a sufficient physical fitness to carry out the training sessions 4. Participants are not included in other sport therapies 5. Participants have to be at least 18 years old 6. Informed consent: Participants provided verbally and written informed consent after they were in detail verbally and written informed about the study and had sufficient time (at least one night) for consideration by given capacity to consent 7. Ability to complete self administered questionnaires in German. 8. Suitability for study-related physical activity by internal medicine preliminary assessment

Exclusion criteria

Exclusion criteria: 1. Serious internistic diseases, particularly cardiopulmonary or musculoskeletal disorders. 2. Manic or hypomanic episodes in the past (bipolar disorder) 3. Pregnant, or breast feeding at the time of assessment 4. Aches and pains at the musculoskeletal system 5. Epilepsy 6. Schizophrenic disorder (F2) 7. Organic, including symptomatic, mental disorders (F0) 8. Judicial hospitalization / lawful support or mentoring

Design outcomes

Primary

MeasureTime frame
Reduction of the depressive symptoms, assessed with the Hamilton Depression Rating Scale, 17 item version (HAMD-17). Four measure time points: baseline (T1), during the intervention (T2), post intervention (T3) and 1-week-follow-up (T4).

Secondary

MeasureTime frame
1. „Skala zur Allgemeinen Selbstwirksamkeitserwartung“ (SWE), self-efficacy, measure time points: T1-T4 2. „Beck-Depressions-Inventar II (BDI-II)“, severity of the depressive symptoms, self rating, measure time points: T1-T4 3. ”Clinical Global Impression“ (CGI), to measure symptom severity and efficacy of the treatment, measure times: T1-T4 4. „ Rated Perceived Exertion“ (RPE), to asses subject's perception of exertion (measure times: first and last day of the trainig and T2). 5. Acceptability of and the attitude to the computer-animated endurance sport with the „Aktzeptanzfragebogen“, measure times: T4 6. Heart rate in all training sessions with a heart rate monitor watch 7. Scores, achieved by the participants in the computer-animated endurance sport 8. Rate of responders 9. Rate of remitters

Countries

Germany

Contacts

Public ContactJennifer Veidt

Schlosspark-Klinik

jennifer.veidt@schlosspark-klinik.de+49 (0)30 3264-1352

Outcome results

None listed

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