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VIBRATION & DEPRESSION – Vibration training to improve depression, quality of life, work ability, pain, motor function and myofascial stiffness: A randomized 6-week intervention study

VIBRATION & DEPRESSION – Vibration training to improve depression, quality of life, work ability, pain, motor function and myofascial stiffness: A randomized 6-week intervention study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00038531
Enrollment
54
Registered
2026-02-17
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

F32.0 F32.1 F32.2

Interventions

Group 1: Experimental group "Vibration Group" & "Treatment As Usual" ("TAU"): n= 27 adult, (partial) inpatient, outpatient patients with a diagnosis of depressive disorder (BDI score: at least 14)
this group receives vibration training 2 to 3 times a week consisting of a single exercise for "stable standing", and the standardized TAU (TAU: guideline-oriented pharmacological treatment, individua
this group receives the standardized TAU
it conducts the same measurements as Arm 1 except for the measurement of immediate well-being right after the vibration training and the Credibility-Expectancy-Questionnaire.

Sponsors

Pädagogische Hochschule Karlsruhe
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The study includes patients with a clinically diagnosed depression (Beck Depression Inventory score of at least 14) who are treated in (partial) inpatient or outpatient settings. Age between 18 and 65 years, normal or corrected vision and hearing, sufficient German language skills.

Exclusion criteria

Exclusion criteria: These include psychotic and bipolar disorders as well as current abuse and dependence on psychoactive substances; individuals under legal guardianship will also be excluded; those diagnosed with thrombosis, hernias, rheumatoid arthritis, epilepsy, unstable gallstones or kidney stones, acute tendon inflammations, pain disorders (this is primarily about pain disorders that can have a negative impact on the implementation of the intervention), or coronary heart disease will also be excluded; pregnancy or breastfeeding are also exclusion criteria.

Design outcomes

Primary

MeasureTime frame
Depressive Symptomatology (Patient Health Questionnaire 9; Engl. original version: Spitzer, Kroenke & Williams, 1999; German translation and validation by Löwe, Zipfel & Herzog, 2003)

Secondary

MeasureTime frame
Measurement of myofascial stiffness on the back (tissue compliance measurements with the IndentoPRO), quality of life (SF-36, Morfeld & Bullinger, 2008), work ability (Work Ability Index, Tuomi et al., 1994), sport motor skills (one-leg stand-test, toe-touch-test, sit-to-stand test), pain (Visual Analog Scale-Pain), immediate well-being directly after vibration training, treatment credibility, and patient expectations regarding treatment success (Credibility-Expectancy Questionnaire, Devilly & Borkovec, 2000).

Countries

Germany

Contacts

Public ContactMarcus Müller

Pädagogische Hochschule Karlsruhe

marcus.mueller@ph-karlsruhe.de+4915253155028

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026