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A Trial of 2 'Point of Care' Diagnostic Methods to Improve Detection and Treatment of Anaemia in African Children (EARS)

Primary Purpose

Anaemia

Status
Completed
Phase
Not Applicable
Locations
Tanzania
Study Type
Interventional
Intervention
Hemocue 210 meter
Copack HBCS
Sponsored by
London School of Hygiene and Tropical Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Anaemia focused on measuring Anaemia, Diagnosis, Primary, Care, Treatment

Eligibility Criteria

undefined - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age under 5 years
  • Pregnancy
  • Suspected anaemia

Sites / Locations

  • Handeni District Health Facilities

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

1

2

3

Arm Description

Hemocue 210 meter

Copack HBCS

Control

Outcomes

Primary Outcome Measures

The proportion of clinic attenders under the age of 5 years who are diagnosed with anaemia (adjusted for anaemia in the community)

Secondary Outcome Measures

Proportion of anaemic children and pregnant women treated for anaemia
Prevalence of anaemia in study communities by age and season
Proportion of clinic attenders referred to the district hospital with Hb> and <8g/dl.
Effectiveness of current MOH anaemia treatment regimens.
Acceptability of HBCS and Hemocue and attitudes to anaemia diagnosis among caretakers and healthworkers
Cost effectiveness of HBC or Hemocue compared to current practice in increasing anaemia diagnosis.

Full Information

First Posted
February 22, 2007
Last Updated
May 26, 2010
Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
National Institute for Medical Research, Tanzania
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1. Study Identification

Unique Protocol Identification Number
NCT00439595
Brief Title
A Trial of 2 'Point of Care' Diagnostic Methods to Improve Detection and Treatment of Anaemia in African Children
Acronym
EARS
Official Title
A Cluster Randomised Trial of Different Methods of Haemoglobin Measurement to Improve Recognition and Treatment of Childhood and Pregnancy-related Anaemia in a Malaria Endemic Area of North East Tanzania.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2010
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
April 2008 (Actual)
Study Completion Date
May 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
London School of Hygiene and Tropical Medicine
Collaborators
National Institute for Medical Research, Tanzania

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A high proportion of children under the age of 5 years and pregnant women in Tanzania is anaemic, particularly in areas of high malaria transmission. The symptoms of anaemia are often non-specific or absent and clinical judgement is generally insensitive in estimating Hb levels, especially in infants who are assessed by basic grade health staff. Thus while treatment for the common causes of anaemia is available, many cases are not treated due to difficulties in recognising anaemia. New diagnostic tools can increase the sensitivity of anaemia detection compared to clinical diagnosis but no studies have demonstrated their effectiveness in increasing case-detection and treatment of anaemic patients at the first level of healthcare. In addition, the costs of their use in relation to any increase in numbers of cases treated are not known and this knowledge is needed to guide public health decisions. Two methods of measuring anaemia are currently suitable for use at the first level of care; Copack Haemoglobin colour scale (HBCS) and Hemocue portable photometry. We propose to compare the effectiveness in basic health facilities of these 2 simple diagnostic tools compared to control dispensaries (current practice) in increasing rates of detection and treatment of anaemia in children under the age of 5 years and pregnant women over the course of 1 year in a cluster-randomised trial in 30 dispensaries in a malaria-endemic area of NE Tanzania.
Detailed Description
Study justification In spite a number of studies describing the sensitivity and specificity of various simple tests for diagnosing anaemia(19-21) there are no studies that have evaluated the effectiveness of basic training of heath workers, use of diagnostic tools and assured availability of anaemia treatments, in reducing the burden of chronic anaemia in children and pregnant women in malaria endemic areas of Africa. The cost-effectiveness of current diagnostic tests is not known and this information is needed to guide public health policy. The rates of diagnosis, treatment and referral from basic health facilities depend on a variety of factors (treatment adherence, clinic attendance, health worker awareness, local prevalence of anaemia etc) that are likely to vary between different areas and health facilities. A cluster randomised study has therefore been designed to shed light on these issues. Design overview This is a cluster randomised open label trial of 2 different 'point of care' diagnostic tools (Hemocue and Copack) to detect anaemia in children under the age of 5 years, each compared to a control arm that will continue current routine practice (based on clinical judgement or ineffective colorimetric methods of measuring haemoglobin). An inherent constraint in designing this effectiveness trial of is the absence of a measure of haemoglobin in control dispensaries. Thus the proportion of children diagnosed with anaemia is the primary outcome and expected rates will be derived from the rolling cross-sectional survey. Children who are referred to the next level of care will be tracked and basic data on the results of investigations and treatment outcome will be recorded. A rolling cross-sectional anaemia survey in children under the age of 5 years will be conducted in the villages served by participating health facilities throughout the trial. Costs of anaemia diagnosis and treatment will be assessed in each of the trial arms and the cost-effectiveness of the intervention arms will each be compared to the control arm in diagnosing and treating anaemia and in normalising haemoglobin levels in children with anaemia. Social surveys (individual interviews and focus group discussions) will be conducted to assess the acceptability and popularity of each of the interventions and to identify treatement-seeking behaviour for and risk factors for anaemia. The results of the trial will be circulated locally and nationally as soon as they are available in order to maximise the usefulness of the results to health planners and providers in Tanzania. An exit strategy at the end of the trial will ensure that any additional resources provided during the trial will be maintained through to the next local health planning and resource allocation cycle.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anaemia
Keywords
Anaemia, Diagnosis, Primary, Care, Treatment

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Hemocue 210 meter
Arm Title
2
Arm Type
Experimental
Arm Description
Copack HBCS
Arm Title
3
Arm Type
No Intervention
Arm Description
Control
Intervention Type
Device
Intervention Name(s)
Hemocue 210 meter
Intervention Description
Diagnostic device
Intervention Type
Device
Intervention Name(s)
Copack HBCS
Primary Outcome Measure Information:
Title
The proportion of clinic attenders under the age of 5 years who are diagnosed with anaemia (adjusted for anaemia in the community)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Proportion of anaemic children and pregnant women treated for anaemia
Time Frame
1 year
Title
Prevalence of anaemia in study communities by age and season
Time Frame
1 year
Title
Proportion of clinic attenders referred to the district hospital with Hb> and <8g/dl.
Time Frame
1 year
Title
Effectiveness of current MOH anaemia treatment regimens.
Time Frame
1 year
Title
Acceptability of HBCS and Hemocue and attitudes to anaemia diagnosis among caretakers and healthworkers
Time Frame
1 year
Title
Cost effectiveness of HBC or Hemocue compared to current practice in increasing anaemia diagnosis.
Time Frame
1 year

10. Eligibility

Sex
All
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age under 5 years Pregnancy Suspected anaemia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hugh Reyburn, MD
Organizational Affiliation
London School of Hygiene and Tropical Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Handeni District Health Facilities
City
Tanga
Country
Tanzania

12. IPD Sharing Statement

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A Trial of 2 'Point of Care' Diagnostic Methods to Improve Detection and Treatment of Anaemia in African Children

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