Clinical Investigation Evaluating the Use of NETSmart Solution , Incorporated to NETSoins Software, in the Care and Support of Elderly People Living in Nursing Homes

NCT07027358 | Terminated

• 1 other identifier: 2024-A00812-45
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

NETSmart software is designed to help doctors, nurses and care assistants adapt the care of elderly people living in nursing homes to the following risks:

• pressure injuries
• undernutrition
• interactions between different drugs
• falls. The software analyzes the information in your medical records, alerts your medical team to any points of vigilance, and suggests appropriate recommendations. The study comprises 2 distinct phases:
• An initial 4-month phase, during which the medical staff will simply assess whether the NETSmart software's recommendations are relevant, without changing their current practice, i.e. they will continue to care for you as usual;
• A second 6-month phase, during which your caregivers will follow the software's recommendations if they feel they are relevant, and potentially adapt your care.

Conditions

Pressure Injury; Fall Prevention; Undernutrition; Drug Interaction

Outcome Measures

Primary Outcomes (1)

• Percentage of clinically relevant recommandations provided by NETSmart

  NETSmart Software provides recommendations to the healthcare professionals. The healthcare professionals are able to mention in the software whether the recommandations are clinically relevant or not. Data will be extracted from the software to analyze this primary outcome.

  4 months

Study Arms (1)

NETSmart

EXPERIMENTAL

Use of NETSmart software by healthcare professionals for these patients

Device: NETSmart software

Interventions

NETSmart software DEVICE

Use of NETSmart software by healthcare professionals

NETSmart

Eligibility Criteria

• Age: 70 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Older Adult (65+)

You may qualify if:

• Male or female, at least 70 years old
• Permanent resident at an investigation site for at least 6 months.
• Considered an at-risk patient, i.e. meeting at least one of the following criteria :
• Braden score \< 16
• At risk of pressure ulcer according to the investigator's judgment
• At risk of undernutrition as judged by the investigator
• Undergoing at least 6 drug treatments
• At risk of falls as judged by the investigator
• Affiliated with the French social security system
• Having given informed, dated and signed consent to participate in the investigation

You may not qualify if:

• Patient with a life expectancy of less than 2 months as judged by the investigator

Sponsors & Collaborators

• Teranga Software: lead
• RCTs: collaborator

Study Sites (1)

Maison de Famille Bourgogne

Étang-sur-Arroux, France

Location

MeSH Terms

Conditions

Pressure Ulcer; Malnutrition

Condition Hierarchy (Ancestors)

Skin Ulcer; Skin Diseases; Skin and Connective Tissue Diseases; Nutrition Disorders; Nutritional and Metabolic Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 19, 2025
• First Posted: June 18, 2025
• Study Start: September 3, 2024
• Primary Completion: February 28, 2025
• Study Completion: April 1, 2025
• Last Updated: June 18, 2025

Record last verified: 2025-06

Locations

FR (1)