Skip to content

Implementation of the Patient-Generated Subjective Global Assessment to screen for malnutrition and risk factors in Nij Smellinghe: applicability and (cost-)effectiveness

Implementation of the Patient-Generated Subjective Global Assessment to screen for malnutrition and risk factors in Nij Smellinghe: applicability and (cost-)effectiveness

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28609
Enrollment
2300
Registered
2018-07-16
Start date
2018-10-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

length of stay, cost-effectiveness, malnutrition, behavior, self-management, awareness, hospital re-admission

Interventions

Screening of risk of malnutrition with the PG-SGA SF. Assessment: full PG-SG. Referral to appropriate health care professional (medical doctor, nurse, dietitian, physiotherapist, speech therapist)

Sponsors

Hanze University of Applied Science Department Healthy Ageing, Allied Health Care and Nursing Nij Smellinghe
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: For the patients to be eligible to participate in this study, a subject must meet all the following criteria: - Aged ≥18 years - Admitted to the Surgery or Lung Disease & Cardiology department - Be able to read and understand Dutch at a moderate level or be able to fill in the PG SGA, if needed with help from family/nurse/nutritional assistant - Be able to understand the experimental procedure and give written consent for filling in the quality of life questionnaire

Exclusion criteria

Exclusion criteria: Participants (patients) will be excluded during the study if he/she: - Has severe cognitive impaired function. This will be evaluated by the professional that hands out the questionnaire. When the patient is not able to fill in the form, even with help from others, then the patient will be excluded

Design outcomes

Primary

MeasureTime frame
The main study parameter is the number (%) of patients screened, assessed, monitored, and treated according to the PG-SGA implementation plan. The number of referrals to several healthcare professionals is also a main study parameter. Additional main parameters are, the knowledge, attitude, acceptance, and perceived practice of the health professionals, and barriers and facilitators of the implementation.

Secondary

MeasureTime frame
Secondary study parameters are PG-SGA SF score, PG-SGA SF category, PG-SGA Global Assessment category, Length of Stay (LOS), Quality of Life (QoL), protein balance at day four, discharge destination, readmission in one month and one year, and cost-effectiveness.

Contacts

Public ContactPriya Dewansingh
p.dewansingh@pl.hanze.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)