A Hybrid Effectiveness/Implementation Trial of the International Guide for Monitoring Child Development

Sponsor
Brigham and Women's Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04665297
Collaborator
Mahatma Gandhi Institute of Medical Sciences (Other), Ummeed Child Development Center (Other), Ankara University (Other), Wuqu' Kawoq, Maya Health Alliance (Other), Harvard Medical School (HMS and HSDM) (Other), University of Washington (Other)
624
2
39.9

Study Details

Study Description

Brief Summary

The aim of this study is to conduct a hybrid effectiveness/implementation assessment of the International Guide for Monitoring Child Development (GMCD) in two LMIC settings, India and Guatemala, within established rural CHW programs. The primary objectives are (a) to evaluate the real-world effectiveness of the GMCD; (b) to use an implementation science framework to understand barriers and facilitators to effective population coverage, provider implementation, and maintenance; (c) to conduct an economic evaluation of the GMCD.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: International Guide for Monitoring Child Development
N/A

Detailed Description

Specific Aim 1: Assess the effectiveness of the GMCD intervention to improve developmental outcomes and nurturing care in India and Guatemala. The investigators will conduct a parallel-arm cluster randomized trial within rural CHW programs. In the primary effectiveness phase, children under 2 years old will receive the GMCD intervention or control for 12 months. Subsequently, control clusters will cross into the intervention, and continue an additional 12 months (total 24 study months). The primary developmental effectiveness outcome will be change in age-adjusted scores at 12 months on the Bayley Scales of Infant Development, 3rd Edition BSID3) (3). The secondary nurturing care effectiveness outcome will be change in mean Home Observation for Measurement of the Environment (HOME) score at 12 months (4).

Specific Aim 2: Assess barriers and facilitators to GMCD implementation using the RE-AIM evaluation framework (5). RE-AIM domains will be assessed as: (a) Reach: participation rates, comparison of participant/non-participant characteristics, attendance/drop-out; (b) Effectiveness: impact on development (BSID3) and nurturing environment (HOME) [in Aim 1]; (c) Adoption: proportion of workers/facilities participating, CHW characteristics; (d) Implementation: contact hours/visit completion, fidelity to delivery protocols; (e) Maintenance: patient outcomes and cost effectiveness analysis at 12-24 months [in Aim 3]; intent by decision makers and implementers to continue intervention. In addition, the investigators will conduct a sequential quantitative-->qualitative explanatory analysis, using interviews and focus groups with implementers from clusters with highest/lowest impact outcomes (BSID3/HOME) to explore institutional inner and outer setting and implementation processes associated with intervention success, using the Consolidated Framework for Implementation Research (CFIR).

Specific Aim 3: Conduct an economic evaluation of the GMCD intervention. Evaluation will assess (a) costs of the interventions at 12 and 24 months; and (b) cost-effectiveness of the intervention (dollar per unit increase in BSID or HOME scores) at 12 months. This analysis will provide cost information to policymakers to help guide resource allocation decisions for ECD interventions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
624 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Nonblinded, two-arm cluster randomized controlled trial for 12 months. At 12 months, control arm crosses into the intervention, and both arms receive the intervention for an additional 12 months (total of 24 months)Nonblinded, two-arm cluster randomized controlled trial for 12 months. At 12 months, control arm crosses into the intervention, and both arms receive the intervention for an additional 12 months (total of 24 months)
Masking:
None (Open Label)
Masking Description:
Given nature of study, blinding is not feasible.
Primary Purpose:
Prevention
Official Title:
An Individualized Approach to Promote Nurturing Care in Low and Middle Income Countries: A Hybrid Effectiveness/Implementation Trial of the International Guide for Monitoring Child Development
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Apr 30, 2026
Anticipated Study Completion Date :
Apr 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention arm

Subjects from intervention clusters will receive the GMCD intervention, delivered in monthly visits to the home by frontline health workers, for 24 months. 0-12 months represents the primary effectiveness study, and 12-24 months a secondary maintenance study.

Behavioral: International Guide for Monitoring Child Development
Monthly GMCD visits includes assessment of risk factors, open-ended exploration of caregiver concerns about development, assessment of functioning in seven developmental domains, and using mutual problem solving strategies to develop a nurturing care plan with the caregiver.

No Intervention: Control Arm

Subjects in control clusters will continue to receive usual care from their frontline health workers. After 12 months (primary effectiveness study) control will cross into the intervention for months 12-24.

Outcome Measures

Primary Outcome Measures

  1. Change in Composite Language Score at 12 months [Change from 0 to 12 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 47-153

  2. Change in Composite Motor Score at 12 months [Change from 0 to 12 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 46-154

  3. Change in Composite Cognitive Score at 12 months [Change from 0 to 12 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 55-145

Secondary Outcome Measures

  1. Change in the Home Observation for Measurement of the Environment Scale (HOME) Raw Score [Change from 0 to 12 months]

    Raw score range 0-45, higher scores better

Other Outcome Measures

  1. Change in Composite Language Score at 24 months [Change from 0 to 24 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 47-153

  2. Change in Composite Motor Score at 24 months [Change from 0 to 24 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 46-154

  3. Change in Composite Cognitive Score at 24 months [Change from 0 to 24 months]

    Using the Bayley Scales of Infant Development, 3rd Edition (BSID3), higher scores better, scale range 55-145

  4. Change in the Home Observation for Measurement of the Environment Scale (HOME) Raw Score [Change from 0 to 24 months]

    Raw score range 0-45, higher scores better

Eligibility Criteria

Criteria

Ages Eligible for Study:
0 Months to 24 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age 0-24 months at the time of enrollment visit

  • receiving health services from frontline health workers of Maya Health Alliance (Guatemala), Mahatma Gandhi Institute (India) or their local partners

Exclusion Criteria:
  • children who are critically ill and are judged by the frontline health worker to require hospitalization or center-based care

  • children whose caregivers do not provide informed consent for the study

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Brigham and Women's Hospital
  • Mahatma Gandhi Institute of Medical Sciences
  • Ummeed Child Development Center
  • Ankara University
  • Wuqu' Kawoq, Maya Health Alliance
  • Harvard Medical School (HMS and HSDM)
  • University of Washington

Investigators

  • Principal Investigator: Peter Rohloff, Assistant Professor/Associate Physician

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Peter J. Rohloff, M.D.,Ph.D., Assistant Professor/Associate Physician, Brigham and Women's Hospital
ClinicalTrials.gov Identifier:
NCT04665297
Other Study ID Numbers:
  • 2020P002143
First Posted:
Dec 11, 2020
Last Update Posted:
Jul 21, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Peter J. Rohloff, M.D.,Ph.D., Assistant Professor/Associate Physician, Brigham and Women's Hospital

Study Results

No Results Posted as of Jul 21, 2022