Substance Use DisorderNCT07168642
A Type I Hybrid Effectiveness-Implementation Trial of MIO
A study testing Mothering from the Inside Out in people with Substance Use Disorder, run by Baystate Medical Center at 1 site in United States.
Trial summary
Mothers with substance use disorders face unprecedented stress in their roles as parents working to care for their children while maintaining healthy recovery. Mothering from the Inside Out (MIO) is the first attachment-based parenting intervention designed specifically for mothers in recovery from substance use… Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Substance Use Disorder
- What is being tested?
- Mothering from the Inside Out
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 200 participants
- Where
- 1 siteUnited States
- Study dates
- 23 Dec 2025to 31 Jul 2029
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Identifies as a woman
- English-speaking
- Age 18 years or older
- Enrolled in outpatient substance use treatment for a substance use disorder (by DSMV criteria) at one of the four target clinics operated by participating agencies
- Caring for at least one child between 0 and 60 months of age (either as guardian or working towards reunification with regular contact)
- Age 5 years or younger
Show all 18Show fewer
- Are in their biological mother's custody OR are in custody of family with the goal of reunification with their biological mother and have permission from the child's legal guardian to participate in this study
- Age 21 years or older
- Employed as an addiction counselor at one of the participating agencies in one of the target clinics
- Have a bachelor's degree or higher in psychology, social work, counseling, or a related field
- Have secure administrative approval for a 1-hour per biweekly commitment to supervision and 2-3 hours weekly for MIO delivery
- Do not intend to give notice and are not scheduled for medical or family leave during the study period
- Willing to have counseling and supervision sessions recorded
- Receive a mean score greater than 4 on the Clinical Reflective Functioning Scale
- Are deemed capable to manage the responsibilities of being a counselor in a randomized trial (deliver MIO promptly to participants, compliant with study procedures and assessments, willing to receive supervision) by their supervisors
- Employment at a participating agency for at least 3 months
- Willingness to complete questionnaires and participate in a confidential interview or focus group
- Fluency in English
Who cannot join
- Have severe mental health problems (e.g., actively suicidal, homicidal, psychosis)
- Severely cognitively impaired
- Have psychiatric or substance-related symptoms requiring inpatient hospitalization or ambulatory detoxification
- Unable to speak English
- Have a potential target child who has a severe medical condition that limits their ability to interact with their mother (such as paralysis or severe weakness)
- Children Subjects
Show all 11Show fewer
- •In child welfare custody and goal is not reunification with biological mother
- Counselor Subjects
- •None
- Agency Staff Subjects
- •None
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Elizabeth Peacock-Chambers, MD, MSc contact
United States1 site, 1 recruiting
- Recruiting
Baystate Medical Center
Springfield, Massachusetts, 01199
Elizabeth Peacock-Chambers, MD, MS, 413-794-8301, elizabeth.peacock-chambers@baystatehealth.org
Briana L Jurkowski, BS, 413-794-8833, briana.jurkowski@baystatehealth.org
About this study
Official title: A Type I Hybrid Effectiveness-Implementation Trial of Mothering From the Inside Out (MIO)
Mothers with substance use disorders face unprecedented stress in their roles as parents working to care for their children while maintaining healthy recovery. Mothering from the Inside Out (MIO) is the first attachment-based parenting intervention designed specifically for mothers in recovery from substance use disorders that has been shown to have benefit for both mother and child in multiple randomized controlled trials. This project will: (a) test the effectiveness of MIO among women in outpatient treatment under 'real-world' conditions, (b) evaluate implementation in different settings, and (c) assess key implementation factors to support optimal uptake and treatment in future dissemination studies; closing an important science-to-service gap for an underserved population in an effort to support maternal and child health simultaneously.
Read the detailed description
Pregnancy and parenting can be life-changing motivators for women with substance use disorders (SUDs) to seek treatment. However, the rate of relapse and overdose for women with SUDs increases sharply after the birth of a child, such that mental health and drug-related deaths are a leading preventable cause of postpartum mortality. Heightened parental stress and lack of adequate parenting supports increase the risk of drug overdose. Mothers with SUDs are also more likely to exhibit maladaptive parenting behaviors associated with long-term developmental, behavioral, and emotional problems in their offspring. Despite the well-established interaction between parenting and SUDs during a critical period, SUD treatment does not systematically include targeted parenting support for mothers in recovery and their young children.
Mothering from the Inside Out (MIO) is an evidence-based, individual parenting intervention designed as an adjunct to outpatient SUD treatment that targets parental reflective functioning, i.e., the capacity to understand behavior, for oneself and one's child, in terms of underlying mental states. MIO has proven bigenerational efficacy in two randomized trials when delivered by researchers under tightly controlled research conditions. Mothers assigned to MIO demonstrated significantly improved parenting capacities and reduced substance use compared with those assigned to parental education.
Although MIO was efficacious when delivered by expert clinicians in highly organized research settings, there are challenges to exporting any evidence-based practice to dynamic real-world environments creating a science-to-service gap. As a first step in addressing these challenges, we successfully trained SUD and mental health counselors to deliver MIO with fidelity in community clinics. Yet, in the only community-based efficacy trial where MIO was delivered by SUD treatment counselors, MIO offered some advantages over parental education with respect to reduction in substance use and depressive symptoms, but MIO did not yield the same magnitude of improvement in parenting as it did in the first two randomized controlled trials.
Community-academic partnerships and governmental funding support in Massachusetts have since allowed our multi-disciplinary team to identify barriers to implementation and develop a practice-informed implementation strategy to mitigate these barriers. We are now poised to simultaneously test the clinical effectiveness of MIO and the utility of our implementation strategy in community-based clinical settings. With guidance from our two community partners, we are proposing a Hybrid Type II research project to test the effectiveness and implementation of MIO as an adjunct to treatment as usual (TAU). SUD counselors (n=16) and mothers enrolled in outpatient SUD treatment (n=200) caring for children ≤5 years of age will be recruited from four SUD treatment clinics operated by two community agencies in Massachusetts. These sites were selected by our community partners based on their generalizability and engagement with parents with SUDs. Mothers will be randomized in a 2:1 fashion to the receipt of either MIO+TAU or TAU to allow for dual examination of the implementation process as well as the MIO mechanism of change. Guided by established frameworks and our implementation conceptual model, we will use a mixed-methods approach to evaluate the relationship between key contextual determinants of MIO implementation. Our specific aims include the following:
Aim 1. Compare the effectiveness of MIO+TAU versus TAU alone. Hypotheses: Compared with mothers receiving TAU, mothers randomized to MIO+TAU will demonstrate a greater increase in parental reflective functioning and greater decrease in parenting stress (primary outcomes) at the end of treatment. They will also demonstrate greater improvement in quality of mother-child interactions and greater decreases in drug use and psychiatric distress (secondary outcomes) at 3-month follow-up.
Aim 2. Assess differences in agency- and clinic-level implementation processes with respect to a) completion of implementation activities, b) tailoring strategies, and c) implementation outcomes.
Hypothesis: Facilitated completion of pre-implementation activities at the agency- and clinic-level will predict greater reach, adoption, feasibility, and fidelity of MIO across four clinical units.
Aim 3. Identify key contextual determinants associated with successful MIO implementation and effectiveness, supported by integration of qualitative and quantitative data to guide large-scale dissemination.
Hypothesis 3a: Primary implementation outcomes (MIO fidelity and feasibility) will be determined by organizational climate, characteristics of individual counselors, and execution of the implementation process integrity.
Hypothesis 3b: The association between primary implementation outcomes (MIO fidelity and feasibility) and secondary effectiveness outcomes (quality of mother-child interactions, maternal drug use, and psychiatric distress) will be mediated by parental reflective functioning and parenting stress (primary effectiveness outcomes).
Moving evidence-based practices into routine care settings is a public health and NIDA priority. When completed, this project will allow us to address the critical gap between research and practice by providing data to support large-scale implementation of MIO in community settings.
- Conditions
- Substance Use Disorder
- Being tested
- Mothering from the Inside Out
- Keywords
- substance use disorder, parenting, parenting intervention, Mothering from the Inside Out, MIO, SUD treatment
- Medical subject headings
- Substance-Related Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Mothering from the Inside OutBehavioural
Mothering from the Inside Out (MIO) is an evidence-based individual psychotherapy designed to help caregivers in recovery build stronger relationships with their children. In MIO, caregivers are helped to build their ability to reflect on their own mental states and how they arose. Often, we find that the thoughts and feelings that drive caregiving behavior are actually triggered by early experiences of being cared for. MIO thus aims to provide a safe, therapeutic space where caregivers' internal experiences are taken seriously and clinicians are genuinely interested, curious, and collaborative. MIO also involves helping caregivers to reflect on the possible mental states underlying their children's behavior. We find that by providing some information about child development through an attachment lens, this can help parents see through their children's eyes and feel less stressed.
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Mothering from the Inside Out (MIO) + treatment as usual (TAU) Receives: Behavioral: Mothering from the Inside Out |
| Control | No intervention | Treatment as usual (TAU) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Parental Reflective Functioning
The Parent Development Interview (PDI) is a semi-structured clinical interview with 19 questions intended to examine parents' representations of their children, themselves as parents, and their relationships with their children. The PDI is coded using an 11-point reflective functioning rating scale (-1 to 9) where higher score indicates higher reflective capacity.
Measured: Baseline, post treatment (week 21)
Parental Reflective Functioning
The Parental Reflective Functioning Questionnaire (PRFQ) is an 18-item questionnaire assessing caregiver's capacity to reflect upon his/her own internal mental experiences as well as those of the child. Uses a 7-point Likert scale with 1 being "Completely disagree," 4 being "Neutral," and 7 being "Completely agree." Items 11 and 18 are reverse coded. Minimum score is 18, max is 126. High scores on this scale indicate serious distortions in parental reflective functioning.
Measured: Baseline, post treatment (week 21)
Parenting Stress
The Parenting Stress Index-Short Form (PSI-SF) is a 36-item questionnaire used to assess parenting stress on a 5-point Likert scale. It's a briefer version of the full Parenting Stress Index, designed to be more efficient for clinical and research settings. The PSI-SF measures three key areas: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child, which together contribute to an overall measure of parenting stress, minimum score 36 and maximum 180. Scores at or above the 85th percentile on the Total Stress scale are considered to be borderline clinically significant.
Measured: Baseline, during treatment (week 13), post treatment (week 21), follow-up (week 33)
Secondary outcomes (9)
Quality of mother-child interaction
The Coding Interactive Behavior (CIB) is a global rating system for analyzing social interactions between two or more partners, in this case, mother and child (videotaped play session with recommended age-appropriate toys). The CIB consists of 33 items (18 relating to the parent, 8 to the child, 5 to the dyad, and 2 focusing on the lead-lag of the interaction) that are rated from 1 (minimal level of behavior) to 5 (maximum level of behavior). Minimum possible score is 33, maximum is 165. A higher score indicates a more positive and adaptive interactive behavior between parent and child.
Measured: Baseline, follow-up (week 33)
Substance Use
Toxicology testing is a method to detect the presence of drugs or other chemicals in a person's urine. This testing is already being completed as a normal procedure by the SUD treatment agencies, and the results on study participants only are shared with the study team on a monthly basis.
Measured: Baseline, monthly during weeks 1-21, post treatment (week 21)
Substance Use
The Timeline Followback (TLFB) is a method to assess recent drug use. It involves asking clients to retrospectively estimate their drug use 7 days to 2 years prior to the interview date. TLFB data can be scored in various ways to quantify different aspects of substance use - for this study, we are looking at whether participants have recent drug use or not.
Measured: Baseline, during treatment (week 13), post treatment (week 21), follow-up (week 33)
Anxiety
The General Anxiety Disorder-7 (GAD-7) is a 7-item screening tool used to assess the severity of generalized anxiety disorder. Each item is rated on a 0-3 scale, with higher scores indicating greater anxiety. Minimum score 0, maximum score 21.
Measured: Baseline, during treatment (week 13), post treatment (week 21)
Depression
The Patient Health Questionnaire-9 (PHQ-9) is a self-administered tool used to screen for and assess the severity of depression. It consists of nine questions, each scored from 0 (not at all) to 3 (nearly every day), with a total possible score ranging from 0 to 27. Higher scores indicate more severe depression, and scores are categorized into ranges to suggest severity levels: minimal (0-4), mild (5-9), moderate (10-14), moderately severe (15-19), and severe (20-27).
Measured: Baseline, during treatment (week 13), post treatment (week 21)
MIO Fidelity
Mothering from the Inside Out - Treatment Fidelity Scales - Revised (MIO-TFS-R) is used to code MIO sessions in frequency and competence across 10 competencies with scores for each competency ranging from 0 to 3. Four of these competencies are MIO-specific, with higher scores on MIO items indicating greater fidelity to the MIO model. For both frequency and competence, the minimum possible overall score is 10 the maximum possible overall score is 30. The minimum score for MIO-specific items is 4, and the maximum is 12.
Measured: Intervention period weeks 4-21
MIO Feasibility
Number of MIO sessions completed in a 16-week period
Measured: After each MIO treatment (week 21 of each mother's participation period)
Organizational Culture
The Organizational Climate Measuring Tool (OCMT) is a standardized scale measuring agency culture. It uses a Likert-type scale of 10 points (1 = maximum disagreement; 10 = maximum agreement) to examine motivation, leadership, and management philosophy.
Measured: Years 1 & 5
Organizational Attitudes
The Evidence-Based Practice Questionnaire (EBPQ) measures individuals' attitudes towards, knowledge of, and implementation of evidence-based practice, and the extent to which barriers may prevent greater uptake of evidence-based practice. The questionnaire contains 24 items scored on a seven-point Likert scale, with lower scores corresponding to poor attitude. There are 3 subscales: practice of evidence-based practice (6 items), attitude towards evidence-based practice (4 items), and knowledge/skills associated with evidence-based practice (14 items).
Measured: Years 1 & 5
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2025
- Study start23 Dec 2025
- Primary completion30 Mar 2029 (estimated)
- Study completion31 Jul 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Substance Use DisorderStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Baystate Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Behavioral Health Network, Spectrum Health Systems
- Responsible party
- Principal investigator, Elizabeth Peacock-Chambers, MD, Baystate Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07168642
- Sponsor's protocol ID
- BH-25-127
- Status last verified
- Jul 2026
- First submitted
- 13 Aug 2025
- Last updated
- 8 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Lowell AF, Peacock-Chambers E, Zayde A, DeCoste CL, McMahon TJ, Suchman NE. Mothering from the Inside Out: Addressing the Intersection of Addiction, Adversity, and Attachment with Evidence-Based Parenting Intervention. Curr Addict Rep. 2021;8(4):605-615. doi: 10.1007/s40429-021-00389-1. Epub 2021 Jul 15.
PubMed 34306964
Study at a glance
From the registry record, last updated by the sponsor on 8 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Type I Hybrid Effectiveness-Implementation Trial of Mothering From the Inside Out (MIO)
- ClinicalTrials.gov ID
- NCT07168642
- Acronym / sponsor ID
- BH-25-127
- Conditions
- Substance Use Disorder
- Keywords
- substance use disorder, parenting, parenting intervention, Mothering from the Inside Out, MIO, SUD treatment
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Baystate Medical CenterUniversity, hospital or other
- Collaborators
- Behavioral Health Network, Spectrum Health Systems
- Study start
- 23 Dec 2025 (actual)
- Primary completion
- 30 Mar 2029 (estimated)
- Study completion
- 31 Jul 2029 (estimated)
- First posted
- 11 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Mothers with substance use disorders face unprecedented stress in their roles as parents working to care for their children while maintaining healthy recovery. Mothering from the Inside Out (MIO) is the first attachment-based parenting intervention designed specifically for mothers in recovery from substance use disorders that has been shown to have benefit for both mother and child in multiple randomized controlled trials. This project will: (a) test the effectiveness of MIO among women in outpatient treatment under 'real-world' conditions, (b) evaluate implementation in different settings, and (c) assess key implementation factors to support optimal uptake and treatment in future dissemination studies; closing an important science-to-service gap for an underserved population in an effort to support maternal and child health simultaneously.
Detailed description
Pregnancy and parenting can be life-changing motivators for women with substance use disorders (SUDs) to seek treatment. However, the rate of relapse and overdose for women with SUDs increases sharply after the birth of a child, such that mental health and drug-related deaths are a leading preventable cause of postpartum mortality. Heightened parental stress and lack of adequate parenting supports increase the risk of drug overdose. Mothers with SUDs are also more likely to exhibit maladaptive parenting behaviors associated with long-term developmental, behavioral, and emotional problems in their offspring. Despite the well-established interaction between parenting and SUDs during a critical period, SUD treatment does not systematically include targeted parenting support for mothers in recovery and their young children.
Mothering from the Inside Out (MIO) is an evidence-based, individual parenting intervention designed as an adjunct to outpatient SUD treatment that targets parental reflective functioning, i.e., the capacity to understand behavior, for oneself and one's child, in terms of underlying mental states. MIO has proven bigenerational efficacy in two randomized trials when delivered by researchers under tightly controlled research conditions. Mothers assigned to MIO demonstrated significantly improved parenting capacities and reduced substance use compared with those assigned to parental education.
Although MIO was efficacious when delivered by expert clinicians in highly organized research settings, there are challenges to exporting any evidence-based practice to dynamic real-world environments creating a science-to-service gap. As a first step in addressing these challenges, we successfully trained SUD and mental health counselors to deliver MIO with fidelity in community clinics. Yet, in the only community-based efficacy trial where MIO was delivered by SUD treatment counselors, MIO offered some advantages over parental education with respect to reduction in substance use and depressive symptoms, but MIO did not yield the same magnitude of improvement in parenting as it did in the first two randomized controlled trials.
Community-academic partnerships and governmental funding support in Massachusetts have since allowed our multi-disciplinary team to identify barriers to implementation and develop a practice-informed implementation strategy to mitigate these barriers. We are now poised to simultaneously test the clinical effectiveness of MIO and the utility of our implementation strategy in community-based clinical settings. With guidance from our two community partners, we are proposing a Hybrid Type II research project to test the effectiveness and implementation of MIO as an adjunct to treatment as usual (TAU). SUD counselors (n=16) and mothers enrolled in outpatient SUD treatment (n=200) caring for children ≤5 years of age will be recruited from four SUD treatment clinics operated by two community agencies in Massachusetts. These sites were selected by our community partners based on their generalizability and engagement with parents with SUDs. Mothers will be randomized in a 2:1 fashion to the receipt of either MIO+TAU or TAU to allow for dual examination of the implementation process as well as the MIO mechanism of change. Guided by established frameworks and our implementation conceptual model, we will use a mixed-methods approach to evaluate the relationship between key contextual determinants of MIO implementation. Our specific aims include the following:
Aim 1. Compare the effectiveness of MIO+TAU versus TAU alone. Hypotheses: Compared with mothers receiving TAU, mothers randomized to MIO+TAU will demonstrate a greater increase in parental reflective functioning and greater decrease in parenting stress (primary outcomes) at the end of treatment. They will also demonstrate greater improvement in quality of mother-child interactions and greater decreases in drug use and psychiatric distress (secondary outcomes) at 3-month follow-up.
Aim 2. Assess differences in agency- and clinic-level implementation processes with respect to a) completion of implementation activities, b) tailoring strategies, and c) implementation outcomes.
Hypothesis: Facilitated completion of pre-implementation activities at the agency- and clinic-level will predict greater reach, adoption, feasibility, and fidelity of MIO across four clinical units.
Aim 3. Identify key contextual determinants associated with successful MIO implementation and effectiveness, supported by integration of qualitative and quantitative data to guide large-scale dissemination.
Hypothesis 3a: Primary implementation outcomes (MIO fidelity and feasibility) will be determined by organizational climate, characteristics of individual counselors, and execution of the implementation process integrity.
Hypothesis 3b: The association between primary implementation outcomes (MIO fidelity and feasibility) and secondary effectiveness outcomes (quality of mother-child interactions, maternal drug use, and psychiatric distress) will be mediated by parental reflective functioning and parenting stress (primary effectiveness outcomes).
Moving evidence-based practices into routine care settings is a public health and NIDA priority. When completed, this project will allow us to address the critical gap between research and practice by providing data to support large-scale implementation of MIO in community settings.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Behavioral: Mothering from the Inside OutMothering from the Inside Out (MIO) + treatment as usual (TAU) |
| Control | No intervention | –Treatment as usual (TAU) |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (18 listed)
- Identifies as a woman
- English-speaking
- Age 18 years or older
- Enrolled in outpatient substance use treatment for a substance use disorder (by DSMV criteria) at one of the four target clinics operated by participating agencies
- Caring for at least one child between 0 and 60 months of age (either as guardian or working towards reunification with regular contact)
Key exclusion criteria (11 listed)
- Have severe mental health problems (e.g., actively suicidal, homicidal, psychosis)
- Severely cognitively impaired
- Have psychiatric or substance-related symptoms requiring inpatient hospitalization or ambulatory detoxification
- Unable to speak English
- Have a potential target child who has a severe medical condition that limits their ability to interact with their mother (such as paralysis or severe weakness)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mothering from the Inside OutMothering from the Inside Out (MIO) is an evidence-based individual psychotherapy designed to help caregivers in recovery build stronger relationships with their children. In MIO, caregivers are helped to build their ability to reflect on their own mental states and how they arose. Often, we find that the thoughts and feelings that drive caregiving behavior are actually triggered by early experiences of being cared for. MIO thus aims to provide a safe, therapeutic space where caregivers' internal experiences are taken seriously and clinicians are genuinely interested, curious, and collaborative. MIO also involves helping caregivers to reflect on the possible mental states underlying their children's behavior. We find that by providing some information about child development through an attachment lens, this can help parents see through their children's eyes and feel less stressed. | Behavioural | Intervention |
Primary outcome
Parental Reflective Functioning
Time frame: Baseline, post treatment (week 21)
The Parent Development Interview (PDI) is a semi-structured clinical interview with 19 questions intended to examine parents' representations of their children, themselves as parents, and their relationships with their children. The PDI is coded using an 11-point reflective functioning rating scale (-1 to 9) where higher score indicates higher reflective capacity.
Parental Reflective Functioning
Time frame: Baseline, post treatment (week 21)
The Parental Reflective Functioning Questionnaire (PRFQ) is an 18-item questionnaire assessing caregiver's capacity to reflect upon his/her own internal mental experiences as well as those of the child. Uses a 7-point Likert scale with 1 being "Completely disagree," 4 being "Neutral," and 7 being "Completely agree." Items 11 and 18 are reverse coded. Minimum score is 18, max is 126. High scores on this scale indicate serious distortions in parental reflective functioning.
Parenting Stress
Time frame: Baseline, during treatment (week 13), post treatment (week 21), follow-up (week 33)
The Parenting Stress Index-Short Form (PSI-SF) is a 36-item questionnaire used to assess parenting stress on a 5-point Likert scale. It's a briefer version of the full Parenting Stress Index, designed to be more efficient for clinical and research settings. The PSI-SF measures three key areas: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child, which together contribute to an overall measure of parenting stress, minimum score 36 and maximum 180. Scores at or above the 85th percentile on the Total Stress scale are considered to be borderline clinically significant.
9 secondary outcomes
Quality of mother-child interaction
Time frame: Baseline, follow-up (week 33)
Substance Use
Time frame: Baseline, monthly during weeks 1-21, post treatment (week 21)
Substance Use
Time frame: Baseline, during treatment (week 13), post treatment (week 21), follow-up (week 33)
Anxiety
Time frame: Baseline, during treatment (week 13), post treatment (week 21)
Depression
Time frame: Baseline, during treatment (week 13), post treatment (week 21)
MIO Fidelity
Time frame: Intervention period weeks 4-21
MIO Feasibility
Time frame: After each MIO treatment (week 21 of each mother's participation period)
Organizational Culture
Time frame: Years 1 & 5
Organizational Attitudes
Time frame: Years 1 & 5
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Jul 2026.
- Background: PubMed 34306964Lowell AF, Peacock-Chambers E, Zayde A, DeCoste CL, McMahon TJ, Suchman NE. Mothering from the Inside Out: Addressing the Intersection of Addiction, Adversity, and Attachment with Evidence-Based Parenting Intervention. Curr Addict Rep. 2021;8(4):605-615. doi: 10.1007/s40429-021-00389-1. Epub 2021 Jul 15.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Elizabeth Peacock-Chambers, MD, MSc contact
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Mothering from the Inside Out in people with Substance Use Disorder, run by Baystate Medical Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 18 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 8 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Elizabeth Peacock-Chambers, MD, MSc (413-794-8301, elizabeth.peacock-chambers@baystatehealth.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Parental Reflective Functioning (time frame: Baseline, post treatment (week 21)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07168642, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jul 2026.