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Investigation into the influence of an exergame and/or VR-based Back training to reduce pain and mobility for chronic back pain in a rehabilitation setting

Investigation into the influence of an exergame and/or VR-based Back training to reduce pain and mobility for chronic back pain in a rehabilitation setting - ICAROS_LBP_Reha

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00035823
Enrollment
52
Registered
2025-12-29
Start date
2025-06-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Individuals with chronic back pain not attributable, upon medical examination, to acute disc herniation, sudden and severe inflammation, vertebral fracture, osteoporosis, tumor, or acute trauma.

Interventions

Group 1: A regular 3-to-4-week inpatient rehabilitation program for chronic back pain, supplemented by 4 sessions of ICAROS Health per week (20–30 minutes per session). Group 2: 3-to-4-week standard i

Sponsors

ICAROS GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Rehabilitation patients with chronic non-specific back pain (medical diagnosis).

Exclusion criteria

Exclusion criteria: Acute disc herniation, sudden or severe inflammation, vertebral fracture, osteoporosis, tumor, acute trauma.

Design outcomes

Primary

MeasureTime frame
Change in pain intensity using the Visual Analog Scale (VAS 0-10) and hip flexibility using the Finger-Floor Distance. These parameters are assessed immediately before and after every single intervention (pre-post design per session) over the entire intervention period of 3 to 4 weeks.

Secondary

MeasureTime frame
Objective core strength; functional disability using the Oswestry Disability Index (ODI); subjective patient satisfaction (comparative questionnaire); assessed at the beginning and end of the study. Additional longitudinal parameters: Well-being using the WHO-5 questionnaire; analgesic intake; device-specific performance parameters (coordination, flexibility, stability) recorded directly via the ICAROS software during application; and adverse events (general condition check); assessed at every single intervention.

Countries

Germany

Contacts

Public ContactKlara Brixius

Deutsche Sporthochschule Köln

Brixius@dshs-koeln.de+49 1516267306

Outcome results

None listed

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