Tool and country | Type of tool and item selection (translation±adaptation) | Reliability | Validity | Comments |
---|---|---|---|---|
Method of assessment | Internal consistency | Criterion | ||
Age | Interobserver | Discriminant | ||
Test-retest | Construct | |||
Kilifi Developmental Checklist (KDC) Kenya28 | Mixture of items from government local screening test, Western tools and LMIC tools developed elsewhere | Excellent* | Items range from poor to good correlation with parental report† | Aimed to be used by low-skilled workers. Identified that secondary school level education was minimal for an assessor. |
Direct and Report | Excellent‡ | |||
11–109 months | Excellent‡ | Done | ||
Kilifi Developmental Inventory (KDI) Kenya30 | Assessment based on KDC with additional items from western tools | Excellent* | Good correlation with maternal reports† | Designed to monitor changes over time. Involved parental focus groups so procedures acceptable to community. |
Direct observation | Excellent‡ | Sensitive to neurodevelopmental disorders and underweight children. | ||
6–35 months | Excellent‡ | |||
Developmental Milestone Checklist Kenya45 | Screening Items from Western tools | Good* | Very good correlation with KDI†.30 | Structured interview. Future plans to develop cut-offs using clinical samples. Can be administered by those with little training. |
Report | Stunted children had lower scores. | |||
3–24 months | Good‡ | Done | ||
Guide to monitoring child development. Turkey46 | Screening Core ideas were adapted from three seminal western models of child development. | Excellent* | Excellent agreement with comprehensive evaluation§ Sensitivity 0.88; 95% CI 0.69 to 0.96 Specificity 0.93; 95% CI 0.83 to 0.97 | Brief, open-ended precoded interview with parent. No specific cognitive domain questions. May not be appropriate for monitoring ‘at-risk’ populations. |
Report | Good§ | |||
0–24 months | ||||
Rapid neurodevelopmental assessment RNA 0–2 years Bangladesh47 | Screening Mixture of neurological examination and neurodevelopment from western tools | Significant differences in scores in children with neurodevelopment impairment | Used in a small high-risk population and identified infants requiring intervention for retinopathy of prematurity. RNA identified additional problems such as impairments in vision and hearing. | |
Direct | Excellent§ | Detected difference in scores between urban rural children in older age groups | ||
0–24 months | ||||
Rapid neurodevelopmental assessment. RNA 2–5 years Bangladesh48 | Screening Mixture of neurological exam and development assessment from western tools | Sensitivity 80–90% Specificity 60–78% | Comparison with ‘gold-standard’ tests already developed for Bangladesh. | |
Direct | Excellent§ | Stunted children had lower scores. | ||
24–60 months | ||||
Malawi Developmental Assessment Tool. Malawi32 | Screening Western developmental tool and new items locally devised | Excellent49 | Good strategy to devise socioemotional items. | |
Direct and report | 60–80% of items at least fair§ | Sensitivity 97% Specificity 82% Sensitive to malnutrition except social developmental domain | ||
0–72 months | 99–100% scoring at least fair§ | Good predictive validity50 51 | ||
INTERGROWTH-21st Neurodevelopment Assessment29 | Screening Items from selection of Western and LMIC tools | Project specific criteria to create a tool for use in children from middle-class and upper class families across low-income, middle-income and high-income settings, carried out by non-specialists. Also evaluates vision, hearing and sleep-wake cycle. | ||
Direct and report | Good | |||
24 months | Excellent | |||
Systematic approach to assess nutritional influences. Indonesia17 | Assessment Items from selection of Western tools | Items at least fair* | Clear hypothesis driven tool creation. May not be suitable as a general developmental assessment. | |
Direct | At least fair agreement¶ | Expected relationship with maternal depression and maternal education | ||
22–55 months | Items at least fair† | |||
Interpretation of statistical tests are listed below.16 52 These need to be interpreted in context of application and population.17 53 | ||||
Levels of κ Levels§, R†, intraclass‡ correlation and α coefficients*. | Level of proposed agreement¶ (%) | Levels of clinical or practical significance | ||
<0.4 | <70% | Poor | ||
0.4–0.59 | 70–79 | Fair | ||
0.60–0.74 | 80–89 | Good | ||
0/75–1.00 | 90–100 | Excellent |
CDAT, child development assessment tool; LMICs, low-income and middle-income countries.