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Directly Observed Iron Supplementation to Treat Anemia (DOHBIT)

Primary Purpose

Iron Deficiency Anemia (IDA)

Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Directly observed home based daily iron therapy
Sponsored by
Build Healthy India Movement
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Iron Deficiency Anemia (IDA) focused on measuring anemia, iron deficiency, nutritional, iron supplementation, cluster randomized control trial

Eligibility Criteria

13 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women and adolescent girls aged 13 years and above who are diagnosed with anemia using WHO defined cut-offs for hemoglobin levels

Exclusion Criteria:

  • Any active medical disease ( acute or chronic)other than anemia, any subject already on iron supplementation for >4 weeks, any subject with significant mental impairment, recent history of Gastrointestinal bleed

Sites / Locations

  • Build Healthy India Movement

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Directly observed home based daily iron therapy

Clinic driven unsupervised daily iron therapy

Arm Description

Village volunteers will provide directly observed home based daily iron supplementation( ferrous sulphate) to enrolled anemic women in the experimental arm

In the control group of villages, clinic driven unsupervised iron ( ferrous sulphate) supplementation will be offered on monthly basis to anemic women for 3 months

Outcomes

Primary Outcome Measures

Prevalence of anemia
Compare the prevalence of anemia in two cluster randomized groups of villages

Secondary Outcome Measures

Compliance with iron therapy
To compare the degree of compliance with iron therapy by anemic women between two cluster randomized groups of villages

Full Information

First Posted
May 22, 2010
Last Updated
May 28, 2011
Sponsor
Build Healthy India Movement
Collaborators
Ministry of Science and Technology, India
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1. Study Identification

Unique Protocol Identification Number
NCT01129843
Brief Title
Directly Observed Iron Supplementation to Treat Anemia
Acronym
DOHBIT
Official Title
A Cluster Randomized Trial for Lowering Prevalence of Anemia in Rural Hilly Villages With Directly Observed Home Based Daily Iron Therapy(DOHBIT)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2011
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
May 2011 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Build Healthy India Movement
Collaborators
Ministry of Science and Technology, India

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
India continues to be one of the countries with very high prevalence of anemia. In fact, National Family Health Survey-3 (NFHS-3,2005-06) revealed increasing prevalence of anemia in women and children, since NFHS-2 in 1998-99. In the backdrop of this alarming trend, the aim of this trial is to assess the effectiveness of a community based anemia management intervention ( curative and holistic) delivered to rural anemia women and girls(aged 13 years and above)in remote hilly villages (unit of randomization) in terms of change in anemia prevalence (unit of analysis) after 3 months of iron supplementation. This trial with a therapeutic component of "Directly Observed Home Based daily Iron Therapy (DOHBIT)" by local village volunteers is conceived as a whole community approach to improve the hemoglobin status of affected patients in remote villages.
Detailed Description
To combat iron deficiency anemia, the challenge is not so much knowing "what" to do, but to understand "how" to implement effective and sustainable interventions. In this perspective, the aim of this trial is to assess the effectiveness of a community based anemia management therapeutic intervention delivered to rural anemic women (aged 13 years and above) in remote hilly villages (unit of randomization) in terms of change in anemia prevalence (unit of analysis) after 3 months of iron supplementation. The intervention programme "Directly Observed Home Based daily Iron Therapy"(DOHBIT) by local village volunteers is conceived as a whole community approach to improve the hemoglobin status of affected patients in remote villages. A cluster-randomized trial will be thus the design of choice from the outset. For intervention arm of trial, each anemic patient will receive DOHBIT (Directly Observed Home Based daily Iron Therapy) by local village volunteer for a total of 90 days whereas in the control arm of trial each patient will receive usual standard iron therapy without daily supervision for the same duration. Information, educational and counseling strategies will be similar for the two groups. Primary outcome will be the anemia prevalence (difference of proportions) in intervention vs. control groups after trial intervention. Secondary outcomes in two groups include mean hemoglobin levels, compliance and side effects of iron therapy, body mass index and quality of life scores. Sample size estimates, adjusted for cluster randomization (assuming Intracluster Correlation Coefficient of 0.05 and mean cluster size of 30 patients/village based on our pilot study), show that with 10 villages, each for intervention and control groups, an average 300 anemic patients per treatment arm would need to be treated to provide sufficient power to determine a 20% difference in anemia prevalence in two groups- a reduction deemed to a worthwhile impact of the intervention to be reliably detected at 80% power. Then a statistically valid approach to the analysis of primary outcome variable will be to calculate a single outcome measure for each randomized unit and apply standard parametric method (chi-square) to the set of summary measures, keeping in mind that any conclusion will be strictly applicable only at the cluster level. Since, covariate adjustment will be required on an individual level for various secondary outcomes, thus a different approach based on the individual, as unit of analysis, adjusting for clustering will be more appropriate in analyzing various secondary outcome measures. Overall, DOHBIT is one of the strategies to increase the capacity of individuals and communities to define, analyze and act to address their own health needs. Moreover, in the supply-demand continuum, DOHBIT by utilizing facilitators and motivators at the local level will optimize demand as well as supply of iron supplementation programme in the community.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Iron Deficiency Anemia (IDA)
Keywords
anemia, iron deficiency, nutritional, iron supplementation, cluster randomized control trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Directly observed home based daily iron therapy
Arm Type
Experimental
Arm Description
Village volunteers will provide directly observed home based daily iron supplementation( ferrous sulphate) to enrolled anemic women in the experimental arm
Arm Title
Clinic driven unsupervised daily iron therapy
Arm Type
Active Comparator
Arm Description
In the control group of villages, clinic driven unsupervised iron ( ferrous sulphate) supplementation will be offered on monthly basis to anemic women for 3 months
Intervention Type
Drug
Intervention Name(s)
Directly observed home based daily iron therapy
Intervention Description
Directly Observed Home based Daily Iron( ferrous sulphate) therapy (DOHBIT) will be provided to the anemic women by the local village volunteers. Dose of elemental iron therapy will be 100 mg once daily for mild to moderate anemia and twice daily for severe anemia for a cumulative duration of 90 days
Primary Outcome Measure Information:
Title
Prevalence of anemia
Description
Compare the prevalence of anemia in two cluster randomized groups of villages
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Compliance with iron therapy
Description
To compare the degree of compliance with iron therapy by anemic women between two cluster randomized groups of villages
Time Frame
1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women and adolescent girls aged 13 years and above who are diagnosed with anemia using WHO defined cut-offs for hemoglobin levels Exclusion Criteria: Any active medical disease ( acute or chronic)other than anemia, any subject already on iron supplementation for >4 weeks, any subject with significant mental impairment, recent history of Gastrointestinal bleed
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Sahul Bharti, MD Pediatrics, PDCC, Dip Stats
Organizational Affiliation
Build Healthy India Movement (BHIM)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Build Healthy India Movement
City
Sirmaur
State/Province
Himachal Pradesh
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
15523164
Citation
Bharti S. Feasibility of "directly observed home-based twice-daily iron therapy" (DOHBIT) for management of anemia in rural patients: a pilot study. Indian J Med Sci. 2004 Oct;58(10):431-8.
Results Reference
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Directly Observed Iron Supplementation to Treat Anemia

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