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Effectiveness of an additional web-based app-intervention to traditional physiotherapy in patients with musculoskeletal pain

Effectiveness of an additional web-based app-intervention to traditional physiotherapy in patients with musculoskeletal pain - HealEN STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00024160
Enrollment
200
Registered
2021-05-03
Start date
2021-06-01
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

musculoskeletal pain

Interventions

Group 1: standard physiotherapy plus 6 months use of the app HealEN Group 2: standard physiotherapy

Sponsors

University of Luebeck
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: ? older than 18 years. ? have an app-enabled smartphone or tablet. ? have musculoskeletal symptoms (lumbar spine and/or cervical spine and/or shoulder and/or hip and/or knee and/or elbow). ? have a referral to outpatient physiotherapy from their doctor. ? have a minimum pain intensity (3/10) OR a minimum of 20% disability (measured with a disease-specific questionnaire (Oswestry Disability Index (ODI), Neck Disability Index (NDI), Disability of the Arm, Shoulder and Hand (DASH), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC))

Exclusion criteria

Exclusion criteria: ? cannot operate a mobile phone/tablet ? do not speak/understand and are not able to read German or English ? have a pathology requiring medical intervention (red flags) ? had surgery within the last six weeks (relevant to the current symptoms) ? suffer from neurological, psychiatric or other diseases that make full participation in the study impossible ? medical interventions are not an exclusion criterion but will be documented

Design outcomes

Primary

MeasureTime frame
Minutes of exercise/physical activity per week documented in an exercise diary; the primary endpoint is 6 weeks after the beginning of the intervention.

Secondary

MeasureTime frame
- region specific disability measured using the WOMAC, Oswestry disability index, neck disability index and DASH - fear of movement (Tampa Skale) - depression (PhQ9) - patient satisfaction

Countries

Germany

Contacts

Public ContactKerstin Luedtke

University of Luebeck

kerstin.luedtke@uni-luebeck.de017621748758

Outcome results

None listed

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