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Validation of the incremental therapeutic effect for patients with back pain by using the Movento (traction bed) medical device during nightly sleep

Validation of the incremental therapeutic effect for patients with back pain by using the Movento (traction bed) medical device during nightly sleep

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025086
Enrollment
110
Registered
2021-04-16
Start date
2021-05-02
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

M42 M47

Interventions

Group 1: The medical device Movento is applied for 21 nights each night for a min. of 5 hours to the audit group. Each patient is treated during the day according to the standards for back rehabilitat

Sponsors

DaThera Consumer Health GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Osteochondrosis / spondylarthrosis, chronification stage 1 and 2 according to Gerbershagen, age > 40 and < 75 years, weight between 40 and 120 kg, height between 150 and 190 cm, good language skills in the German tongue, legal capacity

Exclusion criteria

Exclusion criteria: Disability > 50%, stenosis, existing conflict of interest e.g. accident, post-traumatic stress disorder, work related problems e.g.mobbing, depression, psychosis, discitis, myositis, reumatic thrusts, tumor related indications, radicular lumbar syndrom, radicular dorsal syndrom, radicular cervical syndrom, pregnancy, syringomyelia, open wounds, scin infections, dementia, patients with physical disabilities, alcohol or drug usage, scoliosis

Design outcomes

Primary

MeasureTime frame
Identification of pain improvement on NRS pain scale in comparison to the sole therapy by the standards of the Deutsche Rentenversicherung. Pain intensity is measured on 5 days.

Secondary

MeasureTime frame
Reduction of functional disability by pain (Roland and Morris Disability Questionnaire) and finger ground clearance, reduction start-up time in the morning (questioning patient), Increase of quality of live (SF 36)

Countries

Germany

Contacts

Public ContactChristian Prinz zu Salm-Horstmar

DaThera Consumer Health GmbH

christian.salm@dathera.com+49 172 2364429

Outcome results

None listed

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