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Detection of Anemizations in Primary Care.

Early Detection of Anemizations in Primary Care Using Hemoglobinometer: Randomized Clinical Trial Protocol.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04757909
Acronym
ANHEMOG
Enrollment
33
Registered
2021-02-17
Start date
2017-03-30
Completion date
2023-12-31
Last updated
2021-02-17

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

Conditions

Anemia, Red Blood Cell Transfusion

Keywords

Haemoglobinometry, Primary Care Nursing,, Advanced Practice Nursing

Brief summary

Objective: To evaluate the effect of the use of the hemoglobinometer in primary care on the clinical results of patients with chronic anemia. Methods: The ANHEMOG study is a randomized controlled trial with two parallel arms, intervention and control. It was approved at december 11, 2017. The study randomizes 138 patients with chronic anemia. In the intervention arm, a monthly capillary hemoglobin measurement will be performed with a hemoglobinometer. If a decrease in hemoglobin concentration is detected, an existing transfusion circuit will be followed. Social, demographic and quality of life variables will be collected from all participants. Hypothesis: The results of the research will have an impact on people with chronic anemia who would receive red blood cell transfusion when needed without delay. The improvement in the times of action would reduce decompensations from chronic diseases, visits to the emergency room and hospital admissions, and therefore would improve the quality of life of these patients. Furthermore, the management of the different interventions by the Case Management Nurse (EGC), in this regard, improves the current fragmentation of the different levels of care.

Interventions

DIAGNOSTIC_TESTMonthly Haemoglobinometry

Monthly measurement of capillary hemoglobin with non-invasive techniques in primary health care. Inclusion in a transfusion circuit with referral to a hospital day hospital if necessary.

Sponsors

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

* People over 40 years old * Had received 2 or more red blood cell transfusions due to chronic disease, during a year. * The health provider in Primary Care is the Institut Català de la Salut.

Exclusion criteria

* Presenting kidney failure on hemodialysis treatment. * Being in palliative care situation * Presenting a moderate-severe cognitive impairment, with a Pfeiffer scale score higher than 5. * Not having a caregiver able to detect signs of decompensation.

Design outcomes

Primary

MeasureTime frameDescription
Mean Number of hospital admissions6 and 12 months.Anual mean of hospital admissions caused by haemoglobin concentration decline.
Mean Number of visits to the emergency room6 and 12 months.Anual mean of visits to the emergency room caused by haemoglobin concentration decline.

Secondary

MeasureTime frameDescription
Quality of life self-assessment.6 and 12 months.WHOQOL-BREF questionnaire.
Satisfaction with the intervention.6 and 12 months.Ad-hoc questionnaire.

Countries

Spain

Contacts

Primary ContactBoris Trenado Luengo, RN
btrenado.mn.ics@gencat.cat0034 93384 24 25
Backup ContactPere Toran-Montserrat, MD
ptoran.bnm.ics@gencat.cat003493 741 53 38

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026