- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03589625
Electricity Access and Maternal Care in Rural Health Facilities in Uganda
Evaluation of the Impact of the 'Solar Suitcase' Installation in Healthcare Facilities in Uganda on Quality of Care During Labor and Delivery and Reliability of Electricity
Study Overview
Detailed Description
Ensuring universal access to electricity is essential for global development. In the health sector, lack of reliable light and electricity is a major challenge for health workers when conducting deliveries at night. However, there is very little evidence of the impact of improving access to reliable electrification at maternity facilities on the quality of maternity care they provide.
This stepped wedge cluster-randomized trial will evaluate the impact of a reliable light and electricity source - the "Solar Suitcase" - on outcomes of availability and brightness of light, the quality of maternal care provided, and health worker satisfaction. The study will take place in rural health facilities conducting deliveries in Uganda. The eligible facilities have either no connection to electricity or a modern light source or have reported to have very unreliable light (blackouts occur frequently).
The intervention is a "Solar Suitcase", provided by the non-governmental organization "We Care Solar". The Solar Suitcases are complete solar electric systems that provide essential lighting and power for charging phones and small medical devices. Data collection will include direct observation of deliveries during daytime and nighttime hours, as well as interviews with facility staff. The intervention will be implemented in about 30 facilities in a step process, whereby at each 'step', half of the facilities (selected randomly) will receive the intervention.
Data will be collected at three time points: a baseline period in which no facilities have received the intervention, a midline period in which the first group of facilities has received the intervention but the other half has not, and an endline period in which all facilities have received the intervention.
In addition, facility-level data will be collected at three time points over a 9-month period after the completion of the endline. This data will be used to monitor delivery and ANC volumes at facilities.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Kampala, Uganda
- Innovations for Poverty Action
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
For women delivering at facility:
Inclusion Criteria:
- Pregnant women who are admitted for labor and delivery at participating facilities.
- Women aged 16 years or older.
Exclusion Criteria:
- Pregnant women who present to participating facilities for abortion or abortion-related complications, miscarriage, ectopic pregnancy, antenatal or postnatal complications of pregnancy (not an observation of labor)
- Women who are immediately transferred to another hospital, or are taken straight to surgical theatre (limited or no period of observation possible)
- Women who deliver at home but are brought to the facility for any complication.
- Women who deliver outside the maternity ward or delivery area
- Women who deliver in ambulance while on the way to the facility (woman admitted in the facility for placenta removal)
- Women who have not given consent
- Health worker objects to the observation.
For eligibility of health facility:
Inclusion criteria:
- government health facilities level 2, 3, or 4
- are open 24 hours a day
- conduct deliveries at night
- have unreliable electricity (have either no source of electricity, or have only 1 functional source of electricity and experience blackouts at least several times a week and had power available only sometimes in the past week).
Exclusion criteria:
• facility already has a Solar Suitcase
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Solar Suitcase Installation First Group
Facilities will receive the installation of the Solar Suitcase shortly after baseline data collection.
|
The intervention is a "Solar Suitcase". The Solar Suitcase comes with: 2 LED lights, 1 battery, 1 aluminum glass 100 watt solar panel, 2 rechargeable LED headlamps, 1 universal cell phone charger, 1 USB adapter, 1 fetal Doppler, 1 AA/AAA battery charger and expansion box (provides 2 additional lights). Installers will teach health workers how to use and maintain the Solar Suitcase on the day of installation. Within one week following installation, the contractor will contact the facility over the phone and/or in-person to check if there are any problems with the Suitcase. Additional checks will be made to ensure the solar suitcase is functioning and being used properly. |
Experimental: Solar Suitcase Installation Second Group
Facilities will act as a comparator for experimental group 1 and then will receive the installation of the Solar Suitcase shortly after midline data collection.
|
The intervention is a "Solar Suitcase". The Solar Suitcase comes with: 2 LED lights, 1 battery, 1 aluminum glass 100 watt solar panel, 2 rechargeable LED headlamps, 1 universal cell phone charger, 1 USB adapter, 1 fetal Doppler, 1 AA/AAA battery charger and expansion box (provides 2 additional lights). Installers will teach health workers how to use and maintain the Solar Suitcase on the day of installation. Within one week following installation, the contractor will contact the facility over the phone and/or in-person to check if there are any problems with the Suitcase. Additional checks will be made to ensure the solar suitcase is functioning and being used properly. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Average brightness of room during labor and delivery as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Scale is scored as 1: Very Bright; 2: Somewhat Bright; 3: Dim; 4: Pitch Black.
Variable is binary indicator for "very bright" or "somewhat bright" throughout delivery
|
up to 6 months after installation
|
Satisfactory light source used for entire delivery as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Satisfactory light source is a variable equal to 1 if observation occurs without daylight and facility is using grid, solar or functional generator and zero if using kerosene, candle, torch, etc. Variable is always equal to 1 during daylight.
|
up to 6 months after installation
|
Adequate Light as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Binary variable equal to 1 if light is from a satisfactory source and is "bright" ("very bright" or "somewhat bright") for duration of delivery observation.
|
up to 6 months after installation
|
20-item quality of maternal care index of essential actions to be performed by provider during labor and delivery as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Quality of care index is based on essential actions providers must perform during the course of labor and delivery, as described in Tripathi et al. (2015).
Score is the fraction of 20 items, yielding a range of 0 to 1, with higher scores indicating better quality of maternal care.
|
up to 6 months after installation
|
37-item quality of maternal care index of essential actions to be performed by provider during labor and delivery as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Quality of care index is based on the essential actions providers must perform during the course of labor and delivery, derived from the Maternal and Child Health Integrated Program (MCHIP).
It includes the 20 items from Tripathi et al. (2015) plus an additional 17 quality of care items from MCHIP (2013).
Score is fraction of the 37 items, yielding a range of 0 to 1, with higher scores indicating better quality of maternal care.
|
up to 6 months after installation
|
6-item delays in care index as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Index including: i) Time between facility arrival and first contact with health worker (mins) ii) Time between facility arrival and first assessment (mins) iii) Time between delivery and uterotonic (mins) iv) Time between delivery and assessment of perineal and vaginal lacerations (mins) v) Time between delivery and drying baby with towel (mins) vi) Time between delivery and initiation of breastfeeding (mins) Score is average of the 6 items measured in minutes, with lower values indicating reduced delays in quality of maternal care. Range from 0 to 120 minutes. |
up to 6 months after installation
|
Health Worker Satisfaction with Electricity as measured by health worker survey
Time Frame: up to 6 months after installation
|
Responses on a 1-5 scale with 1: Strongly Disagree, 2: Disagree, 3: Neutral (Neither Agree nor Disagree), 4: Agree, 5: Strongly Agree Worker Satisfaction with Electricity is a binary variable equal to 1 if strongly agree with both: i) I am satisfied with the availability and brightness of light in this facility. ii) I am satisfied with the availability of electricity in this facility |
up to 6 months after installation
|
Overall job satisfaction index as measured by health worker survey
Time Frame: up to 6 months after installation
|
Responses on a 1-5 scale with 1: Strongly Disagree, 2: Disagree, 3: Neutral (Neither Agree nor Disagree), 4: Agree, 5: Strongly Agree Overall job satisfaction index is the mean score (1-5) of the 4 below components: i) These days, I feel motivated to work as hard as I can. ii) Overall, I am satisfied with my job. iii) Overall, the morale level at my department is good iv) I plan on staying at this position for the next year. |
up to 6 months after installation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mean level of brightness over 4 periods of labor and delivery on brightness scale as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Scale is scored as 1: Very Bright; 2: Somewhat Bright; 3: Dim; 4: Pitch Black
|
up to 6 months after installation
|
Minutes of delivery observation without satisfactory light as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Satisfactory light source defined in Primary Outcome 2.
|
up to 6 months after installation
|
Consistent satisfactory light source as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Variable equal to 1 if no interruptions of > 2 hours in satisfactory light source during observed deliveries.
|
up to 6 months after installation
|
Fetal Doppler Use as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Number of times the provider used a fetal doppler during labor and delivery
|
up to 6 months after installation
|
Phone availability as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Phone is available and on for deliveries
|
up to 6 months after installation
|
APGAR Score Assigned as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider assigns any APGAR score (binary variable equal to 1 if provider assigns an APGAR score (range of 0-10), and equal to 0 if no APGAR score is assigned.
|
up to 6 months after installation
|
Basic emergency obstetric care signal functions as measured by facility assessment
Time Frame: up to 6 months after installation
|
Facility reported performance of basic emergency obstetric care signal functions in the past three months. Measure includes the number of signal functions performed from:
|
up to 6 months after installation
|
Basic emergency newborn care signal functions as measured by facility assessment
Time Frame: up to 6 months after installation
|
Facility reported performance of basic emergency newborn care signal functions in the past three months. Measure includes the number of signal functions performed from:
|
up to 6 months after installation
|
Routine obstetric care signal functions as measured by facility assessment
Time Frame: up to 6 months after installation
|
Facility reported universal practice of routine obstetric care signal functions. Measure includes the number of signal functions performed from:
|
up to 6 months after installation
|
Routine newborn care signal functions as measured by facility assessment
Time Frame: up to 6 months after installation
|
Facility reported universal practice of routine newborn care signal functions. Measure includes the number of signal functions performed from:
|
up to 6 months after installation
|
Time between delivery and when suturing began (minutes) as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Observed time between delivery and when provider began suturing lacerations, if needed.
|
up to 6 months after installation
|
4-item quality of suturing index as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Index constructed from the following variables:
|
up to 6 months after installation
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10-item patient treatment index as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Patient treatment/inter-personal quality care index, based on Kruk et al. (2014) including whether health worker: shouted/scolded patient, threatened to withhold treatment, ignored/left patient, did not answer questions, was not present when delivery began, slapped/beat mother, stitched episiotomy without anesthesia, demanded payment inappropriately, requested bribe, did not provide privacy to mother.
Fraction of items that were NOT performed, yielding a range of 0-1, with higher scores indicating better treatment of patients.
|
up to 6 months after installation
|
14-item Partograph Completeness index as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Index of variables (from MCHIP (2013) tool capturing completeness of recording on partograph).
Fraction of 14 items completed on partograph (all binary variables), yielding a range of 0-1, with higher values indicating more completeness.
|
up to 6 months after installation
|
Time between contractions as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between contractions at first exam (mins)
|
up to 6 months after installation
|
Dilation at first exam as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Degree of dilation at woman's first exam (cm)
|
up to 6 months after installation
|
Monthly Delivery Volumes as measured by facility register
Time Frame: up to 6 months after installation
|
Average Number of Monthly Deliveries
|
up to 6 months after installation
|
Monthly Nighttime Delivery Volumes as measured by facility register
Time Frame: up to 6 months after installation
|
Average Number of Nighttime Deliveries per Month
|
up to 6 months after installation
|
Monthly ANC Volumes as measured by facility register
Time Frame: up to 6 months after installation
|
Average Number of Antenatal Clients per Month
|
up to 6 months after installation
|
Monthly Referral Volumes as measured by facility register
Time Frame: up to 6 months after installation
|
Average Number of Monthly Referrals Out of Facility for Mothers and Newborns
|
up to 6 months after installation
|
Sensor Brightness as measured by sensor
Time Frame: up to 6 months after installation
|
Recorded brightness at sensor sight in the two hours around delivery of baby.
|
up to 6 months after installation
|
Depletion of Solar Suitcase Battery Based on Voltage as measured by sensor
Time Frame: up to 6 months after installation
|
Average difference between solar suitcase load voltage in evening and morning (based on sensor)
|
up to 6 months after installation
|
Depletion of Solar Suitcase Battery Based on Charge Time as measured by sensor
Time Frame: up to 6 months after installation
|
Average time between morning and when the solar suitcase is fully charged, based on sensor
|
up to 6 months after installation
|
Solar Suitcase Use for Deliveries as measured by enumerator recorded questionnaire
Time Frame: up to 6 months after installation
|
Fraction of deliveries in which enumerator recorded usage of suitcase
|
up to 6 months after installation
|
Health Worker Assessment of Overhead Light Availability as measured by health worker survey
Time Frame: up to 6 months after installation
|
Health worker response (1-5) on the following scale: 1: No overhead light; 2: Very poor; 3: Poor; 4: Good; 5: Very Good to the question: "In general, how would you rate the availability of overhead light for maternal and newborn care (deliveries) in this facility at night?" |
up to 6 months after installation
|
Health Worker Assessment of Task Light Availability as measured by health worker survey
Time Frame: up to 6 months after installation
|
Health worker response (1-5) on the following scale: 1: No procedure/task light; 2: Very poor; 3: Poor; 4: Good; 5: Very Good to the question: "In general, how would you rate the availability of procedure/task light for maternal and newborn care (deliveries) in this facility at night?" |
up to 6 months after installation
|
Health Worker Assessment of Overhead Light Brightness as measured by health worker survey
Time Frame: up to 6 months after installation
|
Health worker response (1-5) on the following scale: 1: No overhead light; 2: Very poor; 3: Poor; 4: Good; 5: Very Good to the question: "In general, when the overhead light is on, how would you rate the quality of light (brightness) for maternal and newborn care (deliveries) in this facility at night?"
|
up to 6 months after installation
|
Health Worker Assessment of Task Light Brightness as measured by health worker survey
Time Frame: up to 6 months after installation
|
Health worker response (1-5) on the following scale: 1: No procedure/task light; 2: Very poor; 3: Poor; 4: Good; 5: Very Good to the question: "In general, when the procedure/task light is on, how would you rate the quality of light (brightness) for maternal and newborn care (deliveries) in this facility at night?"
|
up to 6 months after installation
|
14-item index of Health worker assessment of impact of blackouts on their ability to perform job functions as measured by health worker survey
Time Frame: up to 6 months after installation
|
Index of items measuring health worker assessment of impact of blackouts in facility on ability to conduct their job, including how often health worker: conducted deliveries without overhead light; had to hold torch in hand to see patient; experienced lack of light that affected normal care provided; delayed care; feared to move around facility; was affected in ability to suture, find/use equipment, conduct examinations of mother, provide emergency care, provide newborn care, monitor fetal heartrate, administer medication, clean up after delivery, manage infection control.
Response to items scored (1-5) on following scale: 1.
Every delivery, 2. Most, 3. Some, 4. Few, or 5. Never.
Overall score measured as average of 14 items, yielding a range of 1-5.
|
up to 6 months after installation
|
Initial exam Bleeding Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider asks whether woman has experienced vaginal bleeding during current pregnancy (binary)
|
up to 6 months after installation
|
Initial exam Headaches/Blurred Vision Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider asks whether woman has experienced headaches and/or blurred vision during current pregnancy (binary)
|
up to 6 months after installation
|
HIV testing as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider offers woman an HIV test or checks her HIV status (binary)
|
up to 6 months after installation
|
Takes Pulse as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider takes pulse of mother during initial exam (binary)
|
up to 6 months after installation
|
Takes Blood Pressure as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider takes both systolic and diastolic blood pressure measurements of mother during initial exam (binary)
|
up to 6 months after installation
|
Wears Sterile Gloves as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider wears sterile gloves for initial vaginal exam (binary)
|
up to 6 months after installation
|
Communication with Patient as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
At least once, explains what will happen in labour to woman and/or her support person.
(binary)
|
up to 6 months after installation
|
Partograph Use as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider starts partograph to monitor progress of labour.
(binary)
|
up to 6 months after installation
|
Hand Washing as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider washes his/her hands with soap and water or uses alcohol hand rub prior to every examination of woman.
(binary)
|
up to 6 months after installation
|
Preparation of Uterotonic as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Uterotonic is prepared for Active Management of the Third Stage of Labor (AMTSL).
(binary)
|
up to 6 months after installation
|
Preparation of Bag and Mask as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Prepares self-inflating ventilation bag and newborn face mask.
(binary)
|
up to 6 months after installation
|
Administration of Oxytocin as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
After delivery, provider administers 10 IU of IM oxytocin, OR:
|
up to 6 months after installation
|
Assessment of Completeness of Placenta as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider assesses completeness of the placenta and membranes.
(binary)
|
up to 6 months after installation
|
Assessment of Lacerations as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Assesses completeness of the placenta and membranes.
(binary)
|
up to 6 months after installation
|
Skin-to-Skin as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider places baby on mother's abdomen or chest skin-to-skin.
(binary)
|
up to 6 months after installation
|
Drying Newborn as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider immediately dries baby with towel.
(binary)
|
up to 6 months after installation
|
Cord Clamping as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider ties or clamps cord.
(binary)
|
up to 6 months after installation
|
Vital Signs Postpartum as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider takes mother's vital signs after delivery.
(binary)
|
up to 6 months after installation
|
Palpation of Uterus as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider palpates uterus after delivery of placenta.
(binary)
|
up to 6 months after installation
|
Breastfeeding within 1 Hour as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Breastfeeding is initiated within one hour of delivery.
(binary)
|
up to 6 months after installation
|
Initial Exam: Previous Pregnancy Inquiry as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider asks about complications during previous pregnancies.
(binary)
|
up to 6 months after installation
|
Initial Exam: Hand Washing as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider washes his/her hands with soap and water or uses alcohol hand rub before initial examination.
(binary)
|
up to 6 months after installation
|
Initial Exam Temperature Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider takes mother's temperature during initial exam.
(binary)
|
up to 6 months after installation
|
Initial Exam Fundal Height Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider checks fundal height during initial exam.
(binary)
|
up to 6 months after installation
|
Initial Exam Fetal Presentation Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider checks fetal presentation by palpation of abdomen.
(binary)
|
up to 6 months after installation
|
Initial Exam Fetal Heart Rate Assessment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider checks fetal heart rate with fetoscope/Doppler/ultrasound.
(binary)
|
up to 6 months after installation
|
Initial Exam: Vaginal Examination as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider performs vaginal examination at initial exam.
(binary)
|
up to 6 months after installation
|
Sterile Gloves for All Exams as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider wears sterile gloves for all vaginal examinations.
(binary)
|
up to 6 months after installation
|
Preparation for Delivery: Cord ties/clamps and sterile scissors/blade as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Prepares disposable cord ties/clamps AND sterile scissors/blade.
(binary)
|
up to 6 months after installation
|
Support of Perineum as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider supports perineum after baby's head is delivered.
(binary)
|
up to 6 months after installation
|
Cord Traction as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Applies traction to the cord while applying suprapubic counter traction.
(binary)
|
up to 6 months after installation
|
Uterine Massage as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider performs uterine massage immediately following the delivery of the placenta.
(binary)
|
up to 6 months after installation
|
Newborn Temperature as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider checks newborn's temperature.
(binary)
|
up to 6 months after installation
|
Assistance with Breastfeeding as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider assists mother with breastfeeding.
(binary)
|
up to 6 months after installation
|
Sterilization of Equipment as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider sterilizes or uses high-level disinfection for all reusable instruments.
(binary)
|
up to 6 months after installation
|
Waste Disposal as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider disposes of all contaminated waste in leak-proof containers.
(binary)
|
up to 6 months after installation
|
Hand Hygiene after Clean Up as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Provider washes his/her hands with soap and water or uses alcohol hand rub after cleaning up.
(binary)
|
up to 6 months after installation
|
Delay in Facility Arrival as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between facility arrival and first contact with health worker (mins)
|
up to 6 months after installation
|
Delay in First Exam as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between facility arrival and first assessment (mins)
|
up to 6 months after installation
|
Delay in Uterotonic as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between delivery and uterotonic (mins)
|
up to 6 months after installation
|
Delay in Assessment for Lacerations as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between delivery and assessment of perineal and vaginal lacerations (mins)
|
up to 6 months after installation
|
Delay in Drying Newborn as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between delivery and drying baby with towel (mins)
|
up to 6 months after installation
|
Delay in Breastfeeding Initiation as measured by observer recorded questionnaire
Time Frame: up to 6 months after installation
|
Time between delivery and initiation of breastfeeding (mins)
|
up to 6 months after installation
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jessica Cohen, PhD, Harvard School of Public Health (HSPH)
- Principal Investigator: Slawa Rokicki, PhD, University College Dublin
Publications and helpful links
General Publications
- Tripathi V, Stanton C, Strobino D, Bartlett L. Development and Validation of an Index to Measure the Quality of Facility-Based Labor and Delivery Care Processes in Sub-Saharan Africa. PLoS One. 2015 Jun 24;10(6):e0129491. doi: 10.1371/journal.pone.0129491. eCollection 2015.
- USAID. Maternal and Child Health Integrated Program (MCHIP), Washington DC: USAID/Jhpiego; 2013.
- Chang W, Cohen J, Mwesigwa B, Waiswa P, Rokicki S. Impact of reliable light and electricity on job satisfaction among maternity health workers in Uganda: A cluster randomized trial. Hum Resour Health. 2022 Mar 29;20(1):30. doi: 10.1186/s12960-022-00722-3.
- Rokicki S, Mwesigwa B, Schmucker L, Cohen JL. Shedding light on quality of care: a study protocol for a randomized trial evaluating the impact of the Solar Suitcase in rural health facilities on maternal and newborn care quality in Uganda. BMC Pregnancy Childbirth. 2019 Aug 22;19(1):306. doi: 10.1186/s12884-019-2453-x.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB-18-0406
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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University of AlbertaGlobal Health Uganda LTDCompleted
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Massachusetts General HospitalMbarara University of Science and Technology; Harvard School of Public Health...CompletedHypertension | Pollution; Exposure | Pollution Related Respiratory DisorderUnited States, Uganda
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University of ArizonaCompletedMelanoma | Renal Cell Carcinoma | HCC | Hepatocellular Carcinoma | Metastatic Cancer | Metastatic Melanoma | Colon Cancer | Differentiated Thyroid Cancer | Metastatic Colon CancerUnited States
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University of ArizonaNational Cancer Institute (NCI)CompletedSun Damaged SkinUnited States
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University of LimerickUniversity Hospital of LimerickCompleted
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University of California, BerkeleySwiss Tropical & Public Health Institute; Universidad de San SimonCompleted
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Council for Scientific and Industrial Research,...Royal College of Surgeons, Ireland; European UnionCompletedDiarrhea | Dysentery (Bloody Diarrhea)South Africa