Research on Emissions, Air Quality, Climate and Cooking Technologies in Northern Ghana (REACCTING)

November 11, 2020 updated by: Michael Hannigan, University of Colorado, Boulder
REACCTING (Research on Emissions, Air quality, Climate, and Cooking Technologies in Northern Ghana) is an interdisciplinary randomized cookstove intervention study in the Kassena-Nankana District of Northern Ghana. The study tests two types of biomass burning stoves that have the potential to meet local cooking needs and represent different "rungs" in the cookstove technology ladder: a locally-made, low-tech Gyapa rocket stove and the imported, highly efficient Philips gasifier stove. Intervention households were randomized into four different groups, three of which received different combinations of two improved stoves, while the fourth group serves as a control for the duration of the study. Diverse measurements assess different points along the causal chain linking the intervention to final outcomes of interest. The investigators assess stove use and cooking behavior, cooking emissions, household air pollution and personal exposure, health burden, and local to regional air quality. Integrated analysis and modeling will tackle a range of interdisciplinary science questions, including examining ambient exposures among the regional population, assessing how those exposures might change with different technologies and behaviors, and estimating the comparative impact of local behavior and technological changes versus regional climate variability and change on local air quality and health outcomes.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

200

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

3 years to 51 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion

Individual Participants:

  • Classified as "rural"
  • Uses biofuel as main cooking fuel source (firewood, animal waste, crop residue/sawdust)
  • Uses borehole as main water source (to facilitate social network analysis linking household's knowledge and attitudes toward stoves to experience of social contacts);
  • Does not have electricity (to permit possible addition of lighting intervention at a later date);
  • Has a woman in household aged 18-55 and at least one child under five (since women and children are the most vulnerable to cookstove smoke and are thus the main focus of our health measures).

Clusters:

  • No more than 25% classified as urban
  • Accessible year-round (determined by field staff)
  • Having at least 10 eligible households (in line with the participant criteria above)

Exclusion:

  • Household could not be located
  • Household declined to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Households enrolled in the control arm of the study did not receive either improved cookstove
Experimental: Gyapa/Gyapa
Households enrolled in the Gyapa/Gyapa arm of the study received two Gyapa stoves for free
Wood stove made in Ghana
Other Names:
  • Rocket stove
Experimental: Gyapa/Philips
Households enrolled in the Gyapa/Philips arm of the study received one Gyapa stove and one Philips stove for free
Wood stove made in Ghana
Other Names:
  • Rocket stove
Philips Smokeless stove HD4012LS
Other Names:
  • Gasifier stove
Experimental: Philips/Philips
Households enrolled in the Philips/Philips arm of the study received two Philips stoves for free
Philips Smokeless stove HD4012LS
Other Names:
  • Gasifier stove

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Health (Biomarkers of inflammation)
Time Frame: At baseline
Health indicators from blood spot samples (C-Reactive Protein, Sicam, sVCAM, serum amyloid A, Interleukin-1b, Interleukin-6, Interleukin-8, tumor necrosis factor alpha).
At baseline
Health (Biomarkers of inflammation)
Time Frame: At 6 months
Health indicators from blood spot samples (C-Reactive Protein, Sicam, sVCAM, serum amyloid A, Interleukin-1b, Interleukin-6, Interleukin-8, tumor necrosis factor alpha).
At 6 months
Health (Biomarkers of inflammation)
Time Frame: At 12 months
Health indicators from blood spot samples (C-Reactive Protein, Sicam, sVCAM, serum amyloid A, Interleukin-1b, Interleukin-6, Interleukin-8, tumor necrosis factor alpha).
At 12 months
Health (Biomarkers of inflammation)
Time Frame: At 18 months
Health indicators from blood spot samples (C-Reactive Protein, Sicam, sVCAM, serum amyloid A, Interleukin-1b, Interleukin-6, Interleukin-8, tumor necrosis factor alpha).
At 18 months
Height
Time Frame: At baseline
Height of participants
At baseline
Height
Time Frame: At 6 months
Height of participants
At 6 months
Height
Time Frame: At 12 months
Height of participants
At 12 months
Height
Time Frame: At 18 months
Height of participants
At 18 months
Weight
Time Frame: At baseline
Weight of participants
At baseline
Weight
Time Frame: At 6 months
Weight of participants
At 6 months
Weight
Time Frame: At 12 months
Weight of participants
At 12 months
Weight
Time Frame: At 18 months
Weight of participants
At 18 months
Mid-arm circumference
Time Frame: At baseline
Measurement of mid-upper arm circumference of participants
At baseline
Mid-arm circumference
Time Frame: At 6 months
Measurement of mid-upper arm circumference of participants
At 6 months
Mid-arm circumference
Time Frame: At 12 months
Measurement of mid-upper arm circumference of participants
At 12 months
Mid-arm circumference
Time Frame: At 18 months
Measurement of mid-upper arm circumference of participants
At 18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Personal exposure to fine particulate matter (PM2.5)
Time Frame: 48 hour deployment periods
48 hour integrated personal PM2.5 concentrations from filter measurements
48 hour deployment periods
Personal exposure to carbon monoxide (CO)
Time Frame: 48 hour deployment periods
Daily average and integrated personal CO concentrations
48 hour deployment periods
Kitchen area concentrations of carbon monoxide (CO)
Time Frame: 48 hour deployment periods
Daily average and integrated kitchen area CO concentrations
48 hour deployment periods
Kitchen area concentrations of fine particulate matter (PM2.5)
Time Frame: 48 hour deployment periods
48 hour integrated kitchen area PM2.5 concentrations from filter measurements
48 hour deployment periods
Self-reported stove usage
Time Frame: At baseline
Surveys administered to respondents (primary cooks)
At baseline
Self-reported stove usage
Time Frame: At 6 months
Surveys administered to respondents (primary cooks)
At 6 months
Self-reported stove usage
Time Frame: At 12 months
Surveys administered to respondents (primary cooks)
At 12 months
Self-reported stove usage
Time Frame: At 18 months
Surveys administered to respondents (primary cooks)
At 18 months
Stove usage as measured by devices
Time Frame: Throughout data collection period, approximately 2 years.
Continuous stove usage indicators as measured by temperature loggers on stoves
Throughout data collection period, approximately 2 years.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2012

Primary Completion (Actual)

December 31, 2016

Study Completion (Actual)

December 31, 2017

Study Registration Dates

First Submitted

September 14, 2020

First Submitted That Met QC Criteria

November 11, 2020

First Posted (Actual)

November 18, 2020

Study Record Updates

Last Update Posted (Actual)

November 18, 2020

Last Update Submitted That Met QC Criteria

November 11, 2020

Last Verified

November 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REACCTING
  • GEO-1211668 (Other Grant/Funding Number: NSF)
  • RD-8354201 (Other Grant/Funding Number: EPA)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

De-identified data are available upon request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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