Table 2.
Overview of constructs and assessments throughout the randomized controlled pilot study protocol
| Construct | Measurement | Description | Intervals assessed | Reference |
|---|---|---|---|---|
| Primary outcomes | ||||
| Feasibility of study | Number of eligible participants, randomized participants, retention and attrition of randomized participants | Baseline, mid-pregnancy, post-program, 3-month postpartum | [65] | |
| Acceptability of IPT | IPT session attendance (≥ 80%), above-average participant IPT program ratings | Post-program | [66] | |
| Secondary Outcomes | ||||
| Social functioning | SAS-SR | 24-item self-report scale of interpersonal functioning in family, friend, romantic, and school or work domains | Baseline, mid-pregnancy, post-program, 3-month postpartum | [67] |
| NRI-BSV | 28-item self-report scale of relationship characteristics for mother, father, peer, and romantic partner relationships | [68] | ||
| Perceived stress | PSS | 14-item self-report scale to assess perception of stress | Baseline, mid-pregnancy, post-program, 3-month postpartum | [69] |
| Depression | CES-D | 20-item self-report scale to assess depression symptoms | Baseline, mid-pregnancy, post-program, 3-month postpartum | [70] |
| EPDS | 10-item self-report scale to assess depression symptoms | Baseline, mid-pregnancy, post-program, 3-month postpartum | [71, 72] | |
| MINI-KID | Structured clinical interview to assess psychiatric disorders, such as major depressive disorder | Baseline, post-program, 3-month postpartum | [73] | |
| Disinhibited eating | EDE | Semi-structured interview to assess disordered eating including objective binge, subjective binge, and objective overeating | Baseline, post-program, 3-month postpartum | [74, 75] |
| EES-C | 25-item self-report questionnaire to assess eating in response to negative emotions | Baseline, mid-pregnancy, post-program, 3-month postpartum | [76] | |
| Physical activity | ActiGraph GT3X+ | Body-worn accelerometer to measure 7 days and nights of habitual physical activity including step counts, light and moderate-vigorous intensity, and sedentary time | Baseline, mid-pregnancy, post-program | [77, 78] |
| Sleep disturbance | ActiGraph GT3X+ | Body-worn accelerometer to measure 7 nights of sleep including total sleep time, sleep onset latency, wake after sleep onset, and sleep efficiency | Baseline, mid-pregnancy, post-program | [79, 80] |
| Body composition | BMI indices | Height and weight measured to calculate BMI | Baseline, mid-pregnancy, post-program, 3-month postpartum | [81] |
| Maternal postpartum adiposity | Body fat | DXA conducted to measure body composition including total fat and lean mass | 3-month postpartum | [82, 83] |
| Maternal insulin sensitivity | WBISI, QUICKI, HOMAIR | 7-sample, 2-h oral glucose tolerance test to estimate insulin sensitivity | 3-month postpartum | [84, 85] |
| Infant adiposity | Body fat | Infant PeaPod conducted to measure body composition including total fat and lean mass | 3-month postpartum | [86] |
Baseline baseline/screening assessment occurring around 12–18 weeks gestation; Mid-Pregnancy mid-pregnancy assessment occurring around 21–28 weeks gestation; Post-Program post-program assessment occurring around 30–34 weeks gestation; 3 Month Postpartum assessment occurring around postpartum week 12; SAS-SR Social Adjustment Scale, Self-Report; NRI-BSV Network of Relationships Inventory-Behavioral Systems Version; PSS Perceived Stress Scale; CES-D Center for Epidemiologic Studies-Depression Scale; EPDS Edinburgh Postnatal Depression Scale; MINI-KID Mini-International Neuropsychiatric Interview for Children and Adolescents; EDE Eating Disorder Examination; EES-C Emotional Eating Scale-Adapted for Children; BMI body mass index (kg/m2, z-score, percentile); DXA dual-energy X-ray absorptiometry; WBISI whole body insulin sensitivity index; QUICKI quantitative insulin sensitivity check index; HOMAIR homeostasis model assessment of insulin resistance