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Effectiveness and Safety of the Nursing Prescription in Acute Health Problems of Low Complexity

F

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina

Status

Unknown

Conditions

Acute Disease

Treatments

Behavioral: Nurse prescription
Behavioral: Medical prescription

Study type

Interventional

Funder types

Other

Identifiers

NCT03892850
4R18/112

Details and patient eligibility

About

Objective: To compare the efficacy/effectiveness of pharmacological nurse prescription with medical prescription in patients attended in a primary care center for minor acute health problems.

Scope of the study: Multicenter study, with the participation of 8 primary care centers of Catalonia.

Methodology: Randomized blind clinical trial, with experimental group receiving pharmacological nurse prescription and a control group receiving medical prescription. Subjects are individuals who request a same day consultation for minor acute pathologies and meet the selection criteria, with random assignment of 374 subjects, 187 per group.

The efficacy/effectiveness of the prescribed treatment will be considered as a no re-attendance during the following 72h and will be completed with the variables: information and knowledge of the treatment, adverse effects, compliance, satisfaction level and resolution of the health problem. The data collection is done 10 days after the visit by an ad-hoc telephone questionnaire of 11 items, previously tested. The analysis is done using the SPSS software version 21.0, obtaining data of descriptive, multivariate and inferential statistics.

Implications for practice: To evidence the equivalence of pharmacological nurse prescription with medical prescription for minor acute health problems

Enrollment

374 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Contusion
  • Diarrhea / vomit
  • Fever without focality
  • Flu
  • Urinary distress
  • Odinophagy
  • Toothache
  • Skin Bite
  • Upper respiratory symptoms
  • Ankle twist

Exclusion criteria

  • Language barrier
  • Cognitive deterioration
  • Sensory deficit
  • Pregnancy
  • Immunosuppression
  • Neoplasia in the last 5 years
  • Does not participate / Does not sign consent
  • Breastfeeding period
  • Reconsult
  • Resides outside of Spain
  • Treatment with glucocorticoids in the last 6 months

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

374 participants in 2 patient groups

nurse prescription
Experimental group
Description:
experimental group receiving pharmacological nurse prescription
Treatment:
Behavioral: Nurse prescription
medical prescription
Active Comparator group
Description:
control group receiving medical prescription
Treatment:
Behavioral: Medical prescription

Trial contacts and locations

0

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Central trial contact

Sonia Fernandez Molero, Nurse; Andres Baiget Ortega

Data sourced from clinicaltrials.gov

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