Antenatal Multiple Micronutrient Supplementation (MMS) in Indonesia

Nutrient Deficiency Clinical Trial

Official title:

Implementation Research to Accelerate Multiple Micronutrient Supplementation During Pregnancy in Indonesia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06225791
• Other study ID #: IRB00016428 / MOD00004017
• Status: Recruiting
• Phase: N/A
• Start date: December 25, 2023
• Est. completion date: December 31, 2025

Study information

• Verified date: January 2024
• Source: Johns Hopkins Bloomberg School of Public Health
• Contact: Trisari Anggondowati, PhD
• Phone: +62 819-9988-1057
• Email: trisari.a[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of this research is to understand how antenatal multiple micronutrient supplements (MMS) can be effectively implemented and scaled within the Indonesian national health system context to support improved maternal nutrition and birth outcomes. Formative research has been conducted to design the implementation strategies that will be tested in this second phase of the study. The objectives are to: - Examine different MMS delivery strategies (i.e., packaging strategies and behavior change communication (BCC) strategies) in relation to MMS adherence. - Assess acceptability, feasibility, fidelity, and coverage of MMS program implementation within antenatal care services (ANC)

Description:

The study will utilize qualitative and quantitative methods to: - Test different MMS delivery strategies (bottle count [90 vs. 180 tablets] and communication strategies [BCC vs. expanded BCC vs. MMS orientation only]) for enhancing supplementation consumption - measured as coverage and adherence. - Assess acceptability, feasibility, and fidelity of MMS program implementation within antenatal care services (ANC) More specifically, the investigators will implement and evaluate different MMS packaging (90 count bottle vs 180-count bottle) strategies and behavior change communication (BCC) strategies. The 3 BCC approaches are further described below. - BCC, BCC without Interpersonal Communication (IPC) strategy is a briefer more basic approach that hopes to improve health care providers knowledge about MMS and the providers ability to communicate with pregnant women. This approach will be rolled out by training one district-level facilitator in each district to become a trainer who will be responsible for training health providers in the corresponding study sub-districts. - Expanded BCC ('BCC with Interpersonal Communication [IPC]') needs more intensive training of master trainers to train health care providers and focuses more on the counselling skills portion. The BCC without IPC is more feasible to implement within the existing system, the investigators anticipate that the BCC with IPC achieve better behavior change results. - MMS Orientation: Women in the control group will receive the existing standard of counselling care. The providers will not be given any sort of training on counselling. Due to the fact that MMS is a new product that the providers will be providing pregnant women, all health care providers will receive a standard MMS orientation so providers are comfortable with the new supplement. The study will be conducted in 25 districts representing the western, central, and eastern regions of Indonesia, Indonesia's socio-cultural diversity, and varying capacity of ANC systems across districts. After selection, the 25 districts were divided to receive high-intensity (8 districts), moderate-intensity (5 districts), or low-intensity (12 districts) evaluation activities with those exposed to high-intensity evaluation efforts having comprehensive individual-level data collected by study employed data collectors while the low-and moderate-intensity district data collection efforts are being done within the context of the existing health system. 1. High intensity evaluation areas (8 districts) Evaluation of MMS acceptability, coverage, adherence, feasibility, and fidelity will include data collection from health professionals and pregnant women by study data collectors, and by ANC monitoring activities. 2. Moderate intensity evaluation areas (5 districts) Evaluation of ANC records with aggregate coverage and adherence numbers will be shared with investigators. In addition, data collectors will collect MMS acceptability, feasibility, and fidelity data within 2 of those 5 districts. 3. Low intensity evaluation area (12 districts) Evaluation of ANC records with aggregate coverage and adherence numbers will be shared with investigators. In addition, a household coverage survey will be administered in a subset of districts (n=6) post-intervention to examine MMS acceptability, adherence, coverage, and implementation feasibility and fidelity. The coverage survey will be designed after 6 months of implementation and will be submitted as a separate application to the Johns Hopkins Bloomberg School of Public Health Institutional Review Board, and a separate entry into Clinicaltrials.gov. Within the 8 high-intensity districts and 5 moderate-intensity districts that are the subject of this Clinicaltrials.gov submission, the study will utilize a three-arm cluster randomized design (with sub-district health center as the unit of randomization).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 3688
• Est. completion date: December 31, 2025
• Est. primary completion date: June 30, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria for 3,360 pregnant women (PW) enrolled from 8 high-intensity evaluation districts (sample group 1)

• Enrolled in ANC 1 through government health facilities.
• Received MMS at ANC 1
• Gestational age at ANC 1 = 20 weeks (verified by health professionals)
• Consent provided to participate in the study. Exclusion Criteria for 3,360 pregnant women (PW) enrolled from 8 high-intensity evaluation districts (sample group 1)
• PW with complicated pregnancy complications (e.g., thalassemia, hemochromatosis,)
• PW planning to move outside study district during study period. Inclusion Criteria for 72 PW / recently delivered women participating in in-depth interviews (IDI) only (sample group 2)
• Enrolled in ANC 1 through government health facilities.
• Received MMS at ANC 1
• Gestational age at ANC 1 = 20 weeks (verified by health professionals)
• Consent provided to participate in qualitative component of study.
• Received MMS for at least 3 months.
• Attended > 2 ANC visits.
• < 4 weeks post-partum Exclusion Criteria for 72 PW / recently delivered women participating in in-depth interviews (IDI) only (sample group 2)
• Enrolled in Sample 1
• Women who are more than 4 weeks postpartum. Inclusion Criteria for 180 healthcare providers participating in focus group discussions (FGDs) (sample group 3)
• Government health workers who provide ANC services (e.g., midwives, general practitioners, and nutritionists)
• Government health facility management staff (e.g., Head of Puskesmas Community Health Clinic, Coordinating Midwife, Head of Pharmacy)
• Willing to give consent to participate in the FGD. Exclusion Criteria for 180 healthcare providers participating in FGDs (sample group 3) • Healthcare Providers who have already participated in a FGD will not be eligible to participate in another FGD Inclusion Criteria for 76 government decision-makers participating in FGD or IDI (sample group 4)
• District-, provincial-, or national-level decision-makers working in nutrition, maternal, newborn and child health, or pharmaceutical roles associated with the antenatal care system in Indonesia.
• Willing to give consent to participate in the FGD or IDI. Exclusion Criteria for 76 government decision-makers participating in FGD or IDI (sample group 4)
• None

Related Conditions & MeSH terms

• Nutrient Deficiency

Intervention

Behavioral:
• MMS (90x2) + BCC or expanded BCC
Provision of 90-count bottles x 2, with enhanced MMS delivery strategy (5 districts with MMS orientation with BCC; 8 districts with MMS orientation with expanded BCC)
• MMS (180x1) + BCC or expanded BCC
Provision of 180-count bottles x 1, with enhanced MMS delivery strategy (5 districts with MMS orientation with BCC; 8 districts with MMS orientation with expanded BCC)

Locations

Country	Name	City	State
Indonesia	Universitas Indonesia	Jakarta

Sponsors (5)

Lead Sponsor	Collaborator
Johns Hopkins Bloomberg School of Public Health	Hasanuddin University, Indonesia University, Universitas Airlangga, Vitamin Angels

Country where clinical trial is conducted

Indonesia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Number of pregnant women being given 180 tablets of MMS	MMS coverage as assessed by the number of pregnant women being given 180 tablets of MMS as compared to the estimated number of pregnant women in the population (e.g., within the 24 study sub-districts) via routine data collection from facility to district health office (aggregate data).	Monthly up to 18 months
Other	Number of MMS tablets consumed	MMS adherence as assessed by the number of MMS tablets (from a total of 180 tablets) women who receive MMS are consuming. Routine Data Collection (aggregate data) from facility to district health office.	Monthly up to 18 months
Primary	MMS Adherence (amount)	The number of MMS tablets (from a total possible 180 tablets) a pregnant woman consumes (sample group 1).	Post-enrollment up to 3 months, Post-pregnancy up to 4 weeks
Primary	MMS Adherence (frequency)	The frequency of which MMS tablets are consumed by a pregnant woman. (sample group 1)	Post-enrollment up to 3 months, Post-pregnancy up to 4 weeks
Secondary	MMS Acceptability among Pregnant Women	The proportion of pregnant women (sample group 1 and 2) who agree with domain-specific statements which reflect different aspects of MMS acceptability (MMS packaging, MMS physical properties, MMS side effects, and MMS counseling using The Theoretical Framework of Acceptability uses a 5-point Likert scale where 5 is "strongly agree" and 1 is "strongly disagree". Score range 5-35, a higher score reflects higher acceptability.	Post-enrollment up to 3 months, Post-pregnancy up to 4 weeks
Secondary	MMS Acceptability among Health Providers assessed by focus group discussions	Healthcare provider acceptability of MMS across multiple domains (e.g., feasibility of delivering counseling and packaging, time burden) (sample group 3). Measured via focus group discussions at two time points during the study (middle and end).	6 months, 12 months
Secondary	Fidelity of providing MMS among Health Providers as assessed by focus group discussions	Administration of an observation checklist (sample group 3),measured via focus group discussions at two time points during the study (middle and end)	6 months, 12 months