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DiPA- a multicenter, controlled, prospective, single-arm, intraindividual study of stabilization or improvement of fall risk measured via the LINDERA Mobility Analysis App in ambulatory care

DiPA- a multicenter, controlled, prospective, single-arm, intraindividual study of stabilization or improvement of fall risk measured via the LINDERA Mobility Analysis App in ambulatory care

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032116
Enrollment
390
Registered
2023-06-21
Start date
2023-06-13
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

Falls, fall risk factors

Interventions

Group 1: Intraindividual comparison design with 3 measurement occasions (T0-T2) two months apart. Data collection from people in need of care in the context of ambulatory care: Control phase T0-T1: U

Sponsors

Lindera GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Seniors :  = 60 years of age  Seniors or legal guardian has understood and agrees to the senior information and consent form Have a care degree (“Pflegegrad”) 2 or 3 Seniors need to be able to stand-up from a chair and walk 3 meters back and forth, either alone or supported by walking aids or a third person Seniors need to have an existing fall risk, based on a screening from the Expert Standard Fall Prevention with the result of at least 2 risk factors for persons in need of care under 65 years and at least 1 risk factor for persons in need of care 65 years and older Connection to an ambulatory care Seniors are capable of providing informed consent to participate in the study Informal caregivers must meet all the following characteristics to be eligible for the study:   Must be giving care to at least one of the participating seniors Good understanding of the German language  Formal caregivers must meet all the following characteristics to be eligible for the study:   The funding institutions and the care facility management as well as the representation of interests (e.g., works council, or employee representatives) are informed about the procedure and agree with the participation to the study  The caregiver training/orientation on the LINDERA Mobility Analysis has been completed Good understanding of the German language

Exclusion criteria

Exclusion criteria: Seniors with any one of the following characteristics are not eligible for study entry:  Seniors with care level degree 1, 4 and 5 Caregivers with any one of the following characteristics are not eligible for study entry:  Lack of understanding of the German language.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is the change of the fall risk score obtained by the LINDERA Mobility Analysis of the seniors. The LINDERA Mobility Analysis was conducted at T0 (start of the control phase), T1 (end of the control phase and start of the intervention phase), and T2 (end of the intervention phase). The Fall Risk Score was acquired at each of these time points.

Secondary

MeasureTime frame
The Short Falls Efficacy Scale International (FES-I). The Short FES-I, a questionnaire aiming to evaluate the fear of falling, was administered at T0 (start of the control phase), T1 (end of the control phase and start of the intervention phase), and T2 (end of the intervention phase). Time spent on complementary support services. These were collected at T0, T1, between T1 and T2 (retrospectively at T2), and at T2.

Countries

Germany

Contacts

Public ContactJürgen Zerth

Katholische Universität Eichstätt - Ingolstadt

Juergen.zerth@ku.de+ 49 08421/9321505

Outcome results

None listed

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