A Scaleable Video Coaching Intervention for Opioid-using Mothers

Sponsor
University of Oregon (Other)
Overall Status
Recruiting
CT.gov ID
NCT04749771
Collaborator
(none)
180
1
2
34.9
5.2

Study Details

Study Description

Brief Summary

This study will adapt and evaluate a novel, innovative, and highly scalable parenting intervention that employs video coaching to target responsive parenting, Filming Interactions to Nurture Development (FIND), among women who have been referred to or are in treatment for opioid misuse/addiction.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Filming Interactions to Nurture Development
  • Behavioral: The Healthy Toddler Program
N/A

Detailed Description

The overall objective of this study is to conduct a randomized trial with a sample of opioid-using women who are in or have been referred for treatment through outpatient and inpatient services and have a child aged 0-36 months. We will use a longitudinal design with an active control condition to test the central hypothesis that associations between (a) increases in responsive caregiving and (b) subsequent caregiver opioid addiction recovery, psychological well-being, and child developmental and biobehavioral outcomes (secondary targets), will be partially mediated through (c) changes in caregiver executive functioning, reward responsiveness, and parent self-concept. The rationale for this work is that it simultaneously addresses the unmet needs of a large, significantly underserved population and allows for a rigorous test of our conceptual model, which specifies hypothesized underlying mechanisms and differential impact.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups. Half of the participants will be randomized into the experimental condition (FIND) while the other half will be randomized into the active control condition (HTP)Two groups. Half of the participants will be randomized into the experimental condition (FIND) while the other half will be randomized into the active control condition (HTP)
Masking:
Single (Participant)
Masking Description:
Research assistants collecting the data during lab visits will not know the condition of the participant and will therefore not be biased during data collection.
Primary Purpose:
Prevention
Official Title:
A Scaleable Video Coaching Intervention for Opioid-using Mothers
Actual Study Start Date :
Jun 4, 2021
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Filming Interactions to Nurture Development (FIND)

FIND is a brief video coaching intervention which involves feedback provided by the coach to the caregiver using brief film clips derived from video of caregiver-child interaction. The coaching focuses on showing caregivers instances in which they are engaging in developmentally-supportive interactions during coaching sessions. FIND is delivered over 10 weekly sessions lasting 30-45 minutes. The process begins with an initial session in which the coach provides an overview, records 10-15 minutes of caregiver-child interaction, then introduces the concept of serve and return. The video is edited to show brief clips in which the caregiver is engaged in the first of five specific caregiver-based components of serve and return. The next week, the FIND coach reviews the edited clips in detail with the caregiver. Sessions continue, alternating between filming and coaching sessions until all five components have been covered sequentially.

Behavioral: Filming Interactions to Nurture Development
FIND is a brief video coaching intervention which involves feedback provided by the coach to the caregiver using brief film clips derived from video of caregiver-child interaction collected in the home.
Other Names:
  • FIND
  • Active Comparator: The Healthy Toddler Program (HTP)

    HTP, the active control intervention, consists of weekly sessions alternating between (a) coaching sessions covering one of five domains of child development (Motor, Cognitive, Language, Play, and Social-Emotional and (b) observation sessions that will include a review of the prior coaching session and an observation and discussion of the caregiver-child interaction. This intervention will consist of 10 sessions each lasting 25-30 minutes. The coach will not engage in any filming or video coaching, but will be able to discuss caregiving concerns. HTP materials are adapted from the Partners for a Healthy Baby curriculum developed by Florida State University's Center for Prevention and Early Intervention Policy.

    Behavioral: The Healthy Toddler Program
    HTP, the active control intervention, consists of weekly sessions alternating between (a) coaching sessions covering one of five domains of child development (Motor, Cognitive, Language, Play, and Social-Emotional and (b) observation sessions that will include a review of the prior coaching session and an observation and discussion of the caregiver-child interaction.
    Other Names:
  • HTP
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence of parenting stress via the Parent Stress Index-IV [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      Items are on a 5-point scale ranging from "strongly agree" to "strongly disagree." Higher scores indicated greater parenting stress. The measures includes three subscales and a total score: Parental distress (12 items) sum score ranging between 12-60 Parent-child dysfunctional interaction (12 items) sum score ranging between 12-60 Difficult child (12 items) sum score ranging between 12-60 Total score (36 items) sum score ranging between 36-180

    2. Caregiver's perceived sense of competency in parenting via the Parent Sense of Competency scale (PSOC) [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The Parenting Sense of Competence (PSOC) questionnaire is filled out by the caregiver to assess parents' sense of competence and enjoyment of parenting. This is an adapted version of the PSOC (original PSOC has 17 items, Johnston & Mash, 1989), with 18 items and simplified language for lower reading levels. These items are answered on a 4-point scale ranging from "strongly agree" to "strongly disagree." Scoring for some items is reversed so that, for all items, higher scores indicate greater parenting self-esteem. Nine (9) items (#s 2,3,4,5,8,9,13,15 and 17) on the PSOC are reverse coded. Subscales include: Satisfaction: Mean score of 2,3,4,5,9,13,15,17, and 18 (Range = 1-4) Efficacy: Mean score of 1,6,7,8,10,11,14, and 16 (Range = 1-4) Total Score: 18 - 72, scored responses summed

    3. Assessment of the caregivers motivation via measurement on the Behavioral Inhibition System and Behavioral Activation System (BIS/BAS) scale [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The BIS/BAS Scale is a 24-item self-report questionnaire designed to measure two motivational systems: the behavioral inhibition system (BIS) and the behavioral activation system (BAS). Participants respond to each item using a 4-point Likert scale. The scale has four subscales. One subscale corresponds to the BIS. Seven items contribute to this score. The remaining three subscales correspond to three components of BAS. BAS Drive measures the motivation to follow one's goals. Four items contribute to this score. BAS Reward Responsiveness measures the sensitivity to pleasant reinforcers in the environment. Four items contribute to this score.

    4. Assessment of emotional or behavioral problems in children as assessed by the SDQ-Infant questionnaire [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The Strengths and Difficulties Questionnaire (SDQ) is a brief behavioural screening questionnaire. 25 items are asked on a 3-point scale from not-true to certainly true. Followed by 5 items assessing difficulties with emotions, concentration, behavior or being able to get along with people.

    5. Measurement of Opioid Craving via Opioid Craving Scale [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The Opioid Craving Scale is a modification of the Cocaine Craving Scale (Weiss et al., 1995, 1997, 2003) used to measure opioid craving. The scale consists of three items rated on a visual analogue scale from 0-10

    6. Self-report of income, occupation and financial strain via the ECHO measure (Income, Occupation, Financial Strain) [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      This measure is a 9-item self-report of income, occupation and financial strain.

    7. Measurement of social support via the Social Support Questionnaire [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      Measures social support, yielding scores for: Perceived number of social supports Satisfaction with social support that is available Questionnaire consists of 27 items with 2-part responses (listing the people they can turn to and rely upon and how satisfied they are with the social supports). Each item is scored based on the number of support persons listed, and the satisfaction scale scored on a scale of 1 to 6 (1 = very satisfied and 6 = very dissatisfied). The overall number and satisfaction scores are summed and divided by 27.

    8. Self-report of commitment and support in regards to family members as assessed by the Cohesion subscale of the Family Enviornment Scale [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The Family Environment Scale (FES) is a self-report 90-item instrument developed to assess the social climates of families focusing on the measurement and description of interpersonal relationships among family members on the directions of personal growth and the basic organizational structure of the family. The Cohesion subscale is a 9-item scale intended to measue the degree of commitment and support that family members provide each other. Respondents rate statements on a scale from mostly true to mostly false.

    9. Communicative skills assessed via the MacArthur Communicative Development Inventories (MCDI) [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The MacArthur Communicative Development Inventories (MCDI) are parent- report instruments for assessing communicative skills in infants and toddlers. The infant form (Level I), designed for children between 8 and 18 months, contains an 89-word vocabulary checklist with separate columns for comprehension and production. There are two equivalent forms of the toddler form (Level II, Forms A and B), both designed for children between 16 and 30 months. Each form contains 100 vocabulary items. Use appropriate norming tables for girls and boys to furnish raw score values for every 5th percentile level from the 5th to the 99th rank.

    10. Observed level of inhibitory control via the Stop Signal Task [Change from baseline at endpoint (3-4 months post-baseline)]

      Inhibitory control will be assessed by the Stop Signal Task (SST) during an MRI scan. The task speed adjusts based on performance and a single response time score will be outputted for each participant. The key neural measure is the degree of blood oxygenation-level dependent (BOLD) signal during stop trials relative to go trials (i.e., the "stop > go" contrast over the entire trial period).

    11. Observed Parental Self-Concept [Change from baseline at endpoint (3-4 months post-baseline)]

      The PSET involves visual presentation of single words or short phrases in the parenting domain (e.g., kind, supportive, enforces rules) seen under two different instruction conditions. The identity condition will ask participants to indicate via a button press whether the word or phrase describes them as a parent (left index finger = yes, right index finger = no). The control condition will ask participants to indicate via a button press whether the word or phrase is a quality that can change for a parent (yes/no). Scores are percent endorsement of developmentally-supportive (DS) and developmentally-unsupportive (DU) items in each condition. The key neural contrasts are neural activation during the presentation of (a) identity > control trials and (b) identity-yes > identity-no trials.

    12. Coded rate of responsive caregiving via conversational turns [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      Conversational turns is a simple coding scheme designed to record timing, quantity, and length of caregiver and child utterances.

    13. Assessment of parent's warmth and hostility towards their child through the use of the Iowa Family Interaction Rating Scales [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      The Iowa family interaction rating scales were used to assess parent's warmth and hostility towards their partner, their perceived warmth and hostility received from their partner, and warmth and hostility towards their child. The questionnaire is divided into 3 parts; the first 10 questions ask how you have behaved towards your partner, the next 10 ask how your partner has behaved towards you, and the final 10 questions ask how you have behaved towards your child. There are 2 scales for each part of the questionnaire, warmth (6 items) and hostility (4 items). For both scales each item has a possible 7 responses. Each scale reverse scored and then summed by adding each item score, giving a possible range of 0-42 for the warmth scale and 0-28 for the hostility scale. Higher scores indicate higher levels of warmth/hostility respectively.

    Secondary Outcome Measures

    1. Mobile Messaging for Responsive Caregiving (MMRC) [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      Caregiver's self-reported rate of responsive caregiving interactions between child and caregiver.

    2. Demographic information [Baseline]

      Demographic information including socioeconomic status, age and sex of caregiver and child, education level, race/ethnicity

    3. Incidence of early adversity assessed via the Adverse Childhood Experiences (ACEs) [Baseline]

      The ACE is a 10-item measure of childhood adversity and is often used as a predicter of poorer outcomes later in life. The higher the score out of 10, the more likely for poor outcomes. Sum the scores of all responses 1-10 for total ACE score. Reverse code the emotional neglect question, question 10, which counts as an ACE if either sub-question is answered "No." The developers suggest not including the supplemental questions in the Total ACE score. They recommend remaining true to the original ACE 10 categories so we can compare data across sites. If desired, you can sum the scores on the supplementary questions, and create a supplementary grand total to examine separately. TotalACES=total ACE score TotalSupp=sum of supplemental questions TotalAll=Sum of ACE score and supplemental question score

    4. Assessment of mental health domains across psychiatric conditions via the use of the PhenX Broad Psychopathology questionnaire [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      This measure consists of 23 questions that assess 13 psychiatric domains, including depression, anger, mania, anxiety, somatic symptoms, suicidal ideation, psychosis, sleep problems, memory, repetitive thoughts and behaviors, dissociation, personality functioning, and substance use. Each item inquires about how much (or how often) the individual has been bothered by the specific symptom during the past 2 weeks.

    5. Intervention Fidelity assessed through use of a fidelity criteria rubric [Assessed at the conclusion of the intervention, directly before endpoint (3-4 months post-baseline)]

      Intervention Fidelity is assessed by the number of required items completed from a checklist of required actions for the given intervention.

    6. Intervention Dosage as assessed by number of sessions complete [Assessed at the conclusion of the intervention, directly before endpoint (3-4 months post-baseline)]

      Intervention Dosage is assessed by the number of completed sessions for each intervention. Total FIND Sessions Complete = Count of sessions complete (0-10) Total HTP Sessions Complete = Count of sessions complete (0-10)

    7. Assessment of unpredictability and fragmentation of early-life environments in infants and children through the use of the Questionnaire of Unpredictability in Childhood (QUIC) [At Baseline]

      The QUIC, a reliable and valid self-report assessment of exposure to unpredictability in the social, emotional, and physical domains during early life, is a brief, comprehensive, and promising instrument for predicting risk for mental illness. The QUIC consists of an overall score and five separate subscale scores. Higher scores indicate more exposure to unpredictability in childhood. To obtain the overall score or subscale scores, reverse score select items (indicated by an R after the item number) and then calculate the sum of the items in each scale: Parental monitoring and involvement = 1R + 3R + 4R + 5R + 6R + 7R + 9R + 10R + 14R Parental predictability = 2 + 8R + 11 + 12 + 15R + 16 + 17R + 31 + 32 + 33 + 34 + 35 Parental environment = 18 + 19 + 21 + 22 + 28R + 29 + 30 Physical environment = 13 + 20 + 26 + 27 + 36R + 37 + 38 Safety and security = 23 + 24 + 25 Overall = Sum of all subscales.

    8. Self-reported substance use and treatment history as assessed by questionnaire modified from PhenX and iOpen [Change from baseline at endpoint (3-4 months post-baseline) and 6 months post-endpoint]

      Questionnaire developed from PhenX and iOpen to assess substance use and treatment history.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Must be an adult (18 years or older) mother with a child between the ages of 0-36 months

    • Must be in or have been referred for treatment due to maternal opioid use

    • Mother must have custody of child at least half-time each week at study entry

    Exclusion Criteria:
    • Metal implants, metal fragments, pacemakers, or other electronic medical implants

    • Claustrophobic

    • Weigh > 550 lbs

    • Women who are or think they may be pregnant

    • History of neurological disorders

    • Left-handed

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Oregon Eugene Oregon United States 97403

    Sponsors and Collaborators

    • University of Oregon

    Investigators

    • Principal Investigator: Philip A Fisher, Ph.D., University of Oregon

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of Oregon
    ClinicalTrials.gov Identifier:
    NCT04749771
    Other Study ID Numbers:
    • 256792
    First Posted:
    Feb 11, 2021
    Last Update Posted:
    Jun 30, 2022
    Last Verified:
    Jun 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 University of Oregon
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 30, 2022