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Preparation of a clinical report on anonymized, statistically evaluated Data from a retrospective data collection on the clinical efficacy of the CE-marked Vivira app "Therapeutic exercise program for home use"

Preparation of a clinical report on anonymized, statistically evaluated Data from a retrospective data collection on the clinical efficacy of the CE-marked Vivira app "Therapeutic exercise program for home use" - Vivira RStudy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00021785
Enrollment
179
Registered
2020-08-25
Start date
2020-06-01
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

M17.0 M54.5 M53.2 M53.8 M53.9 M54.6 M54.8 M54.9 M99.02 M99.03 M99.04 M99.82 M99.83 M99.84 M99.92 M99.93 M99.94 M42.0 M42.1 M42.9 M16.0 M99.85 M99.86 M99.95 M99.96 M25.55 M25.85 M25.95 M99.86 M99.96 M25.56 M25.86

Interventions

Group 1: Retrospective recording of treatment using the Vivira app. It is an intra-individual control: i.e. the study is single-arm, the control is the preliminary (= historical) findings of the same

Sponsors

Vivira Health Lab GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients which are • patients with chronic pain of the musculoskeletal system • and baseline pain score of 1 or more as from Jan. 09, 2018 and later

Exclusion criteria

Exclusion criteria: • Patients who were not able to follow the exercise protocol. • Patients with severe vision problems • No pain, pain score=0 • Discontinuation with no pain value following week 2: these patients were considered as trial users but not as ITT-users. • Non-premium users: these patients are also considered as test users and not as ITT-users. These were test users trying Vivira only for a few days for free. • prescription of analgetics • acute malignant disease • Dementia • drug or alcohol abuse • Previous use of a movement therapy DiGA (Vivira, Kaia, etc.) • limited legal capacity • significantly impaired vision or blindness • serious internal disorders (condition after heart attack, severe organ failure, need for dialysis, etc.) • serious neurological disorders (stroke, paralysis, multiple sclerosis, convulsions, etc.) • rheumatic disease • Osteoporosis • Pregnancy • Bleeding tendency / haemophilia • Gait insecurity and frequent falls • acute herniated disc or other disorder with radiation to the legs (radiculopathy, sensorimotor failure) • Herniated disc in the past • Spinal column infection in the past or acute • Spine OP • Spinal tumor • Injury of the spinal column • Joint replacement (TEP) or partial joint replacement • Osteotomy (an operation to correct the axis of the leg) • joint infection in the past or acute • free joint body • Osteochondrosis dissecans or bone necrosis • Injury to the knee or hip joint • Hip Dysplasia • Arthrodesis (joint stiffening) in one of the two knee or hip joints • Acute instability of the knee or hip joint • Knee or hip surgery in the last year • clinically relevant bone marrow edema

Design outcomes

Primary

MeasureTime frame
Pain VNRS (validated numerical-verbal rating scale) after 12 weeks

Secondary

MeasureTime frame
Proprietary functional test

Countries

Germany

Contacts

Public ContactPhilip Heimann

Vivira Health Lab GmbH

philip@vivira.com+4915140732078

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 10, 2026