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Intravenous Antibiotic Treatment at Home

Intravenous Antibiotic Treatment at Home: A New Model for Across Services Interaction With the Use of Welfare Technology and Telemedicine.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04898452
Acronym
Hosp@Home
Enrollment
19
Registered
2021-05-24
Start date
2020-07-02
Completion date
2027-04-01
Last updated
2026-08-24

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

Conditions

Infection

Keywords

Home Care Services, Hospital-Based, Telemedicine, Home Infusion Therapy, Hospital at home, Antibiotics

Brief summary

The purpose of the study is to develop and evaluate a new model for across services interaction with the use of welfare technology and telemedicine. The model includes innovative and new routines for the exchange of patient information, quality systems and procedures between the municipality and the hospital. This model will first be tested for use in intravenous antibiotic therapy. The results of the study will be used to further develop the service. In the larger context, it is desirable to provide knowledge that is transferable to other diagnostic groups, treatment methods and geographical areas.

Detailed description

This research-based innovation study has an evaluation approach with follow-up evaluation as the overall approach. The pre-project was carried out with a qualitative approach under the auspices of SINTEF 2018/2019. The main project consists of sub-study 1 and sub-study 2 (2020/2022). Sub-study 1: The project use an iterative, user-centered service methodology with a qualitative approach. Here, SINTEF has the main responsibility for a qualitative summary after conducting interviews, observations and group discussions with patients, next of kins and health professionals regarding the development and testing / quality assurance of the new concept / service course for home treatment. Sub-study 2: The approach here is quantitative. Descriptive data must be obtained from the hospital and municipal patient records, patient administration system (PAS) at Kristiansund hospital, alarm data from the Regional Response Center and pump log from the individual patient's infusion pump after home treatment.

Interventions

OTHERA new model of interaction across health services with use of welfare technology and telemedicine

Instead of admitted to the hospital, patients are followed up at home by the municipal regional response center and nurses in the response team according to the individual treatment plan. Hospital physicians are medically responsible throughout the course.

Sponsors

Helse Møre og Romsdal HF
Lead SponsorOTHER_GOV
SINTEF Health Research
CollaboratorOTHER
Kristiansund municipality
CollaboratorUNKNOWN
Centre for Health Innovation
CollaboratorUNKNOWN
Hospital Pharmacy of Central Norway Trust
CollaboratorUNKNOWN

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Main or bi-diagnosis during stay: A692 Borreliosis G00 - G009 Central nervous system inflammatory disorders I33 Endocarditis J86 Empyema D46.3 Spondylodiscitis M86 Osteomyelitis T84 Prosthesis / osteosynthesis infections M00.0-M00.9 Pyogen / septic arthritis J40-J47 Chronic diseases of the lower respiratory tract * Competent to give consent * The infection can not be treated with oral antibiotics in monotherapy * Selected IV antibiotics must be suitable for administration via selected pumps * The patient's condition is stable and does not require frequent observation by health care professionals * The patient is motivated and willing to participate in intravenous treatment in home hospitals * Must, after training, demonstrate mastery of practical procedures related to pump handling and any other procedures described in the patient's treatment plan * The home must be suitable for intravenous antibiotic treatment; access to refrigerators, hygienic conditions, social conditions * The patient must have a mobile phone and be able to handle the system for fast and secure communication with the Regional Response Center (RRO)

Exclusion criteria

* consent not given

Design outcomes

Primary

MeasureTime frameDescription
number of rehospitalisations45 months
patient satisfaction45 monthsassessed with semi-structured interview
health personnel's opinion on patient safety45 monthsbased on answers in web-case-registration-form (CRF)

Countries

Norway

Contacts

STUDY_DIRECTORTorstein Hole, md phd

Møre og Romsdal Hospital Trust

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 25, 2026