Non-communicable Diseases (NCD)ENABLENCT07442318
Enabling Environments for Non-communicable Disease Risk Reduction in Ethiopia
A study testing Structured lifestyle counseling integrated into ANC and Standard routine ANC in people with Non-communicable Diseases (NCD), run by Norwegian Institute of Public Health at 4 sites in Ethiopia.
Trial summary
The ENABLE study focuses on pregnant women attending routine antenatal care (ANC) in urban primary health care facilities in four Ethiopian cities. Many women in this setting face increased health risks due to unhealthy diets, low physical activity, and exposure to air pollution which can affect both maternal and… Read more about this study
- Who is it for?
- Ages 18 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Non-communicable Diseases (NCD)
- What is being tested?
- Structured lifestyle counseling integrated into ANC and Standard routine ANC
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,268 participants
- Where
- 4 sitesEthiopia
- Study dates
- 11 May 2026to May 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Pregnant women aged 18 years or older
- Gestational age ≤20 weeks at the time of enrollment
- Residing in one of the four study cities (Addis Ababa, Adama, Harar, or Jimma)
- Attending their first antenatal care visit at one of the participating public health facilities
- Willing and able to provide informed consent
Who cannot join
- Pregnant women identified as high risk at enrollment, including those with pre-existing medical conditions, or other conditions requiring specialized care and who cannot continue receiving standard routine ANC.
Trial locations and contacts
4 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Ethiopia4 sites, 4 recruiting
- Recruiting
Adama
Adama, Oromiya
Hanna Berhane, +251 11 639 0000, hannayemane@addiscontinental.edu.et
Hanna Berhane
- Recruiting
Addis Ababa
Addis Ababa, Addis Ababa
Masresha Tessema, +251 11 213 3499, dr.masresha.tessema@gmail.com
Masresha Tessema
- Recruiting
Harar
Harar, Harare
Kedir Roba, +251 025 666 1881, kedir.t.roba@gmail.com
Kedir Roba
- Recruiting
Jimma
Jimma, Oromiya
Gudina Terefe, +251 094 120 5177, gudina.terefe@ju.edu.et
Gudina Terefe
About this study
Official title: Enhancing Non-Communicable Disease Prevention Among Pregnant Women Through Healthy Lifestyle Promotion in Four Urban Sites in Ethiopia: A Cluster Randomized Controlled Trial in Primary Health Care Facilities
The ENABLE study focuses on pregnant women attending routine antenatal care (ANC) in urban primary health care facilities in four Ethiopian cities. Many women in this setting face increased health risks due to unhealthy diets, low physical activity, and exposure to air pollution which can affect both maternal and newborn health and increase the risk of non-communicable diseases (NCDs) later in life.
In this study, pregnant women in intervention health centers receive structured, tailored counseling as part of their regular ANC visits. This counseling supports healthier eating, physical activity and reduced exposure to air pollution. Health care providers, including health workers in health centers and Urban Health Extension Professionals (UHEPs), are trained to deliver this counseling supported by a digital ANC eRegistry for clinical decision-making, which enhances adherence to national guidelines, and strengthens the quality of care. Facilitators further strengthen the intervention's implementation by ensuring fidelity to counseling protocols and by adapting content to the Ethiopian urban health system context.
Read more
The study hypothesis is that integrating lifestyle counseling into routine ANC will improve maternal health behaviors and pregnancy outcomes, and reduce NCD risk among pregnant women, compared with standard routine ANC alone.
By embedding NCD prevention within routine maternal health services, the ENABLE study aims to strengthen the role of ANC as a platform for early prevention and long-term health benefits for women and their children.
Read the detailed description
The ENABLE study is a two-arm, parallel-group, cluster-randomized controlled trial (cRCT) designed to address the rising burden of NCDs in Ethiopia by integrating NCD risk reduction counseling into routine ANC.
The investigators will evaluate the effectiveness and implementation of an integrated ANC-based intervention for reducing NCD risk factors during pregnancy in urban Ethiopia. The trial follows a Hybrid Type II effectiveness-implementation design, simultaneously assessing effectiveness on improving birth outcomes, specifically birth weight, and evaluating implementation processes under routine primary health care conditions.
The study will be conducted in 77 public urban health centers in four Ethiopian cities: Addis Ababa, Adama, Harar, and Jimma. Health centers and their catchment areas constitute the unit of randomization (clusters)," and are allocated in a 1:1 ratio to the intervention or control arm using covariate-constrained randomization to ensure balance by facility size and baseline ANC caseload. The trial will enroll 1,268 pregnant women (approximately 19 per cluster) who are attending their first routine ANC visit at ≤20 weeks of gestation. The women will be followed up through delivery.
The ENABLE intervention integrates structured counselling on three modifiable NCD risk factors, namely unhealthy diet, physical inactivity, and exposure to air pollution, into routine ANC services. The intervention is designed to be delivered within existing health care delivery systems by health workers and UHEPs within routine service workflows. Counseling follows the WHO 5As behavior change model (Ask, Advise, Assess, Assist, Arrange) which is based on WHO's brief intervention ("BRIEF project"), national ANC guidelines, and other relevant national recommendations and has been adapted to the local context.
Based on previous knowledge and formative work, the intervention is implemented through three tailored implementation strategies:
- Facilitation: Trained facilitators provide ongoing support and collaborative problem-solving around intervention delivery to health workers and UHEPs to strengthen counseling skills and ensure fidelity to the intervention. ii) Digital ANC eRegistry: A digital tool, adapted from the WHO Digital Adaptation Kit, supports standardized screening, clinical decision support, documentation, automates SMS reminders for patients, and routine monitoring of service quality and outcomes at the point of care. iii) Training: Health workers in intervention facilities receive targeted training on NCD risk screening, counseling delivery, and use of the digital ANC eRegistry to promote sustainable integration of NCD prevention within routine maternal health services.
Health centers randomized to the control arm continue to provide standard routine ANC according to national guidelines, without access to ENABLE training, facilitation or the digital ANC eRegistry.
The primary effectiveness outcome is newborn birth weight. Other outcomes include maternal dietary quality, physical activity, behaviors related to indoor air pollution exposure, and quality of ANC service delivery and NCD-related screening and counseling practices. Implementation outcomes include feasibility, acceptability, appropriateness, fidelity, and contextual determinants of implementation. Data are collected using structured surveys, routine digital records, and qualitative methods (focus group discussions and interviews).
Additionally, a biomarker sub-study will examine early-life biological pathways associated with early NCD risks by analyzing maternal and newborn blood and urine samples from a subset of participants.
- Conditions
- Non-communicable Diseases (NCD)
- Being tested
- Structured lifestyle counseling integrated into ANC, Standard routine ANC
- Keywords
- Antenatal care, Pregnancy, Primary Health Care, Behavioral Counseling, Digital Health, Chronic Disease Risk Factors, Health Promotion, Dietary Behavior, Physical Activity, Air Pollution, Health Services Research, Clinical Decision Support Systems
- Medical subject headings
- Noncommunicable Diseases, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Structured lifestyle counseling integrated into ANCBehavioural
The intervention is delivered throughout pregnancy beginning at enrollment. The intervention is implemented through three context tailored strategies: health worker training, facilitation, and a digital ANC eRegistry.
The ENABLE intervention integrates structured counseling on three modifiable non-communicable disease (NCD) risk factors into routine antenatal care (ANC), to promote healthy dietary behaviors, physical activity, and behaviors related to exposure to air pollution during pregnancy, aiming to improve maternal and newborn outcomes.
Facility and community-based health workers counsel pregnant women during scheduled ANC visits and through community outreach contacts by Urban Health Extention Proffesionals (UHEPs).
Standard routine ANCBehavioural
Standard routine antenatal care (ANC) as defined by the Ethiopian national ANC guidelines. This includes standard clinical assessments, counseling and follow-up provided during pregnancy.
| Study group | Role | What they receive |
|---|---|---|
| ENABLE Intervention arm | Experimental | Pregnant women in the intervention arm receive antenatal care (ANC) at health centers implementing the ENABLE intervention. In addition to routine ANC, health workers in health centers allocated to this arm integrate structured counseling on three modifiable non-communicable disease (NCD) risk factors during pregnancy, supported by implementation strategies. Participants are followed from enrollment through delivery, with outcome data collected during routine care and scheduled study assessments. Receives: Behavioral: Structured lifestyle counseling integrated into ANC |
| Control arm | Active comparator | Pregnant women in the control arm receive standard routine antenatal care (ANC) according to the Ethiopian national guidelines at health centers assigned to the control group. Unlike the intervention group, the control group does not receive the ENABLE multicomponent package, therefore health workers at these health centers are not provided with ENABLE facilitator-supported counseling, training or digital tools. Participants are followed from enrollment through delivery, with outcome data collected during standard routine care and scheduled study assessments. Receives: Behavioral: Standard routine ANC |
What is being measured
The primary outcome is the main question the study is designed to answer.
Birth weight
Birth weight of the newborn measured in grams within 24 hours of delivery using calibrated scales and recorded in the routine register or digital ANC eRegistry.
Measured: At delivery (within 24 hours)
Secondary outcomes (5)
Dietary Behavior
Dietary behaviors are assessed using diet quality indicators, including dietary diversity score, minimum dietary diversity for women (MDD-W), Global Dietary Recommendation (GDR) score, NCD risk scores measured by the Diet Quality Questionnaire. In a subsample of participants selected for biomarker collection, multiple-pass 24-hour dietary recalls will be conducted to derive Global Diet Quality Score, adherence to the Ethiopian Food-Based Dietary Guidelines, and mean probability of adequacy of micronutrients based on dietary intake. In the same subsample, maternal biological samples will be collected and analyzed for selected biochemical markers of micronutrient deficiencies.
Measured: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Physical activity
Physical activity is assessed using self-reported measures of frequency, duration and intensity of activities (both physical activity and sedentary activities) during pregnancy, using the Pregnancy Physical Activity Questionnaire. In a sub-sample physical activity is additionally assessed using wearable activity monitors to record movement and sedentary time.
Measured: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Air pollution exposure-related behaviors
Behaviors related to air pollution exposure are assessed using a composite index capturing the adoption of recommended practices to reduce household and environmental air pollution during pregnancy. In a subsample of participants, household air quality is objectively assessed using air pollution monitoring devices to estimate indoor air pollutant levels.
Measured: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Quality of NCD counseling during ANC
Fidelity to the delivery of the counseling on NCD risk factors during ANC and its perceived quality is assessed through structured surveys with pregnant women attending ANC services in both intervention and control facilities. Measures capture the content, frequency, and perceived quality of counseling related to diet, physical activity, and air pollution during pregnancy.
Measured: Three occasions, i.e., baseline, and at 12 and 18 months after facilitation has commenced. The last measurement includes a 6-month follow-up after completing the facilitation component.
Quality of ANC related to NCDs
Quality of ANC assessed using routine service delivery indicators reflecting appropriate screening and management of pregnancy-related conditions associated with NCD. Indicators include the proportion of pregnant women appropriately screened and managed for anemia, gestational diabetes, gestational hypertension, and maternal malnutrition, assessed using mid-upper arm circumference (MUAC) and body mass index (BMI). Data are derived from routinely collected ANC records in both intervention and control facilities.
Measured: Baseline, and at 12 months after implementation has commenced
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Mar 2026
- Study start11 May 2026
- Primary completion10 Apr 2027 (estimated)
- Study completionMay 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Non-communicable Diseases (NCD)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants are assigned to study arms using a parallel-group, cluster-randomized design. Urban public health centers constitute the unit of randomization. Clusters are allocated in a 1:1 ratio to either the intervention or control arm and remain in their assigned group for the duration of the study.
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 1,268 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Norwegian Institute of Public Health
- Sponsor type
- Other government
- Collaborators
- Ethiopian Public Health Institute, Addis Continental Institute of Public Health, Jimma University, Haramaya Unversity, Lund University, University of Oslo, Uppsala University, Vital Strategies, Aveiro University
- Responsible party
- Sponsor
- Investigators
- Masresha Tessema, PhD, Principal investigator, Ethiopian Public Health InstituteEleni Papadopoulou, PhD, Principal investigator, Norwegian Institute of Public Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07442318
- Sponsor's protocol ID
- EPHI-IRB-607-2025
- Other IDs
- 101137232
- Acronym
- ENABLE
- Status last verified
- May 2026
- First submitted
- 27 Jan 2026
- Last updated
- 28 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Fully anonymised individual participant data generated in the ENABLE trial will be made available to other researchers. Data will be de-identified prior to sharing, with all direct and indirect identifiers removed. Access to the data will be managed through the institutional data repository of the Ethiopian Public Health Institute (EPHI) following a formal application and approval process.
Study at a glance
From the registry record, last updated by the sponsor on 28 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Enhancing Non-Communicable Disease Prevention Among Pregnant Women Through Healthy Lifestyle Promotion in Four Urban Sites in Ethiopia: A Cluster Randomized Controlled Trial in Primary Health Care Facilities
- ClinicalTrials.gov ID
- NCT07442318
- Acronym / sponsor ID
- ENABLE / EPHI-IRB-607-2025
- Conditions
- Non-communicable Diseases (NCD)
- Keywords
- Antenatal care, Pregnancy, Primary Health Care, Behavioral Counseling, Digital Health, Chronic Disease Risk Factors, Health Promotion, Dietary Behavior
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,268 participants (estimated)
- Lead sponsor
- Norwegian Institute of Public HealthOther government
- Collaborators
- Ethiopian Public Health Institute, Addis Continental Institute of Public Health, Jimma University, Haramaya Unversity, Lund University, University of Oslo, Uppsala University, Vital Strategies, Aveiro University
- Study start
- 11 May 2026 (actual)
- Primary completion
- 10 Apr 2027 (estimated)
- Study completion
- May 2027 (estimated)
- First posted
- 2 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The ENABLE study focuses on pregnant women attending routine antenatal care (ANC) in urban primary health care facilities in four Ethiopian cities. Many women in this setting face increased health risks due to unhealthy diets, low physical activity, and exposure to air pollution which can affect both maternal and newborn health and increase the risk of non-communicable diseases (NCDs) later in life.
In this study, pregnant women in intervention health centers receive structured, tailored counseling as part of their regular ANC visits. This counseling supports healthier eating, physical activity and reduced exposure to air pollution. Health care providers, including health workers in health centers and Urban Health Extension Professionals (UHEPs), are trained to deliver this counseling supported by a digital ANC eRegistry for clinical decision-making, which enhances adherence to national guidelines, and strengthens the quality of care. Facilitators further strengthen the intervention's implementation by ensuring fidelity to counseling protocols and by adapting content to the Ethiopian urban health system context.
The study hypothesis is that integrating lifestyle counseling into routine ANC will improve maternal health behaviors and pregnancy outcomes, and reduce NCD risk among pregnant women, compared with standard routine ANC alone.
By embedding NCD prevention within routine maternal health services, the ENABLE study aims to strengthen the role of ANC as a platform for early prevention and long-term health benefits for women and their children.
Detailed description
The ENABLE study is a two-arm, parallel-group, cluster-randomized controlled trial (cRCT) designed to address the rising burden of NCDs in Ethiopia by integrating NCD risk reduction counseling into routine ANC.
The investigators will evaluate the effectiveness and implementation of an integrated ANC-based intervention for reducing NCD risk factors during pregnancy in urban Ethiopia. The trial follows a Hybrid Type II effectiveness-implementation design, simultaneously assessing effectiveness on improving birth outcomes, specifically birth weight, and evaluating implementation processes under routine primary health care conditions.
The study will be conducted in 77 public urban health centers in four Ethiopian cities: Addis Ababa, Adama, Harar, and Jimma. Health centers and their catchment areas constitute the unit of randomization (clusters)," and are allocated in a 1:1 ratio to the intervention or control arm using covariate-constrained randomization to ensure balance by facility size and baseline ANC caseload. The trial will enroll 1,268 pregnant women (approximately 19 per cluster) who are attending their first routine ANC visit at ≤20 weeks of gestation. The women will be followed up through delivery.
The ENABLE intervention integrates structured counselling on three modifiable NCD risk factors, namely unhealthy diet, physical inactivity, and exposure to air pollution, into routine ANC services. The intervention is designed to be delivered within existing health care delivery systems by health workers and UHEPs within routine service workflows. Counseling follows the WHO 5As behavior change model (Ask, Advise, Assess, Assist, Arrange) which is based on WHO's brief intervention ("BRIEF project"), national ANC guidelines, and other relevant national recommendations and has been adapted to the local context.
Based on previous knowledge and formative work, the intervention is implemented through three tailored implementation strategies:
- Facilitation: Trained facilitators provide ongoing support and collaborative problem-solving around intervention delivery to health workers and UHEPs to strengthen counseling skills and ensure fidelity to the intervention. ii) Digital ANC eRegistry: A digital tool, adapted from the WHO Digital Adaptation Kit, supports standardized screening, clinical decision support, documentation, automates SMS reminders for patients, and routine monitoring of service quality and outcomes at the point of care. iii) Training: Health workers in intervention facilities receive targeted training on NCD risk screening, counseling delivery, and use of the digital ANC eRegistry to promote sustainable integration of NCD prevention within routine maternal health services.
Health centers randomized to the control arm continue to provide standard routine ANC according to national guidelines, without access to ENABLE training, facilitation or the digital ANC eRegistry.
The primary effectiveness outcome is newborn birth weight. Other outcomes include maternal dietary quality, physical activity, behaviors related to indoor air pollution exposure, and quality of ANC service delivery and NCD-related screening and counseling practices. Implementation outcomes include feasibility, acceptability, appropriateness, fidelity, and contextual determinants of implementation. Data are collected using structured surveys, routine digital records, and qualitative methods (focus group discussions and interviews).
Additionally, a biomarker sub-study will examine early-life biological pathways associated with early NCD risks by analyzing maternal and newborn blood and urine samples from a subset of participants.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
- Model description
- Participants are assigned to study arms using a parallel-group, cluster-randomized design. Urban public health centers constitute the unit of randomization. Clusters are allocated in a 1:1 ratio to either the intervention or control arm and remain in their assigned group for the duration of the study.
| Arm | Type | Receives |
|---|---|---|
| ENABLE Intervention arm | Experimental | Behavioral: Structured lifestyle counseling integrated into ANCPregnant women in the intervention arm receive antenatal care (ANC) at health centers implementing the ENABLE intervention. In addition to routine ANC, health workers in health centers allocated to this arm integrate structured counseling on three modifiable non-communicable disease (NCD) risk factors during pregnancy, supported by implementation strategies. Participants are followed from enrollment through delivery, with outcome data collected during routine care and scheduled study assessments. |
| Control arm | Active comparator | Behavioral: Standard routine ANCPregnant women in the control arm receive standard routine antenatal care (ANC) according to the Ethiopian national guidelines at health centers assigned to the control group. Unlike the intervention group, the control group does not receive the ENABLE multicomponent package, therefore health workers at these health centers are not provided with ENABLE facilitator-supported counseling, training or digital tools. Participants are followed from enrollment through delivery, with outcome data collected during standard routine care and scheduled study assessments. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Pregnant women aged 18 years or older
- Gestational age ≤20 weeks at the time of enrollment
- Residing in one of the four study cities (Addis Ababa, Adama, Harar, or Jimma)
- Attending their first antenatal care visit at one of the participating public health facilities
- Willing and able to provide informed consent
Key exclusion criteria (1 listed)
- Pregnant women identified as high risk at enrollment, including those with pre-existing medical conditions, or other conditions requiring specialized care and who cannot continue receiving standard routine ANC.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Structured lifestyle counseling integrated into ANCThe intervention is delivered throughout pregnancy beginning at enrollment. The intervention is implemented through three context tailored strategies: health worker training, facilitation, and a digital ANC eRegistry. The ENABLE intervention integrates structured counseling on three modifiable non-communicable disease (NCD) risk factors into routine antenatal care (ANC), to promote healthy dietary behaviors, physical activity, and behaviors related to exposure to air pollution during pregnancy, aiming to improve maternal and newborn outcomes. Facility and community-based health workers counsel pregnant women during scheduled ANC visits and through community outreach contacts by Urban Health Extention Proffesionals (UHEPs). | Behavioural | ENABLE Intervention arm |
| Standard routine ANCStandard routine antenatal care (ANC) as defined by the Ethiopian national ANC guidelines. This includes standard clinical assessments, counseling and follow-up provided during pregnancy. | Behavioural | Control arm |
Primary outcome
Birth weight
Time frame: At delivery (within 24 hours)
Birth weight of the newborn measured in grams within 24 hours of delivery using calibrated scales and recorded in the routine register or digital ANC eRegistry.
5 secondary outcomes
Dietary Behavior
Time frame: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Physical activity
Time frame: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Air pollution exposure-related behaviors
Time frame: Baseline (enrollment) and third trimester of pregnancy (≥28 weeks of gestation)
Quality of NCD counseling during ANC
Time frame: Three occasions, i.e., baseline, and at 12 and 18 months after facilitation has commenced. The last measurement includes a 6-month follow-up after completing the facilitation component.
Quality of ANC related to NCDs
Time frame: Baseline, and at 12 months after implementation has commenced
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 May 2026.
- Individual participant dataSharing planned: Yes. Fully anonymised individual participant data generated in the ENABLE trial will be made available to other researchers. Data will be de-identified prior to sharing, with all direct and indirect identifiers removed. Access to the data will be managed through the institutional data repository of the Ethiopian Public Health Institute (EPHI) following a formal application and approval process.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Masresha Tessema, PhD principal investigator
Ethiopian Public Health Institute
Eleni Papadopoulou, PhD principal investigator
Norwegian Institute of Public Health
4 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Structured lifestyle counseling integrated into ANC and Standard routine ANC in people with Non-communicable Diseases (NCD), run by Norwegian Institute of Public Health at 4 sites in Ethiopia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 28 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 4 sites in Ethiopia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Masresha Tessema, PhD (+251919782082, dr.masresha.tessema@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Birth weight (time frame: At delivery (within 24 hours)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 May 2026.