MedPath

DBT-P Treatment Study

Not Applicable
Not yet recruiting
Conditions
Emotion Dysregulation
Registration Number
NCT06963801
Lead Sponsor
Duke University
Brief Summary

The goal of this study is to find out if improving emotion regulation skills use during pregnancy reduces maternal stress and improves heart rate.

The main questions it aims to answer are:

* Does improving emotion regulation skills during pregnancy reduce stress and improve the ability to cope?

* How is a participant's heart rate affected by their ability to control their emotions during pregnancy?

Researchers will test the hypothesis that dialectical behavior therapy skills groups (DBT-P) will improve emotion regulation skills use as well as heart rate.

Participants will:

* Visit the clinic for 3 sessions at the beginning, middle and end of their pregnancy.

* Compete surveys and interviews asking about their thoughts, feelings and how they cope with emotions.

* Have their heart rate taken.

* If assigned to the investigational group, they will complete weekly remote emotion regulation skills groups for 10 weeks and complete daily diary cards that ask about mood and any thoughts of self-harm.

Detailed Description

The investigators' observational research with mothers with emotion dysregulation and their infants shows that poor emotion regulation skill use is a mechanism that likely confers risk for self-injurious thoughts and behaviors, depression, and anxiety in the mother and neurobehavioral and co-regulatory challenges in the infant. Emotion dysregulation is an impairing, early-emerging, transdiagnostic vulnerability factor that has intergenerational implications. Treatments have been developed for non-pregnant adults with emotion dysregulation but these are costly, time-intensive, and do not address the unique needs of pregnant people, highlighting an unmet therapeutic need. Through this innovative intervention, researchers will test whether targeting emotion regulation skills use during pregnancy will both improve postpartum emotion regulation, newborn neurobehavior, and mother-infant co-regulation. Early identification of the mechanisms implicated in risk. The researchers will deliver 10 weeks of DBT skills classes selected and adapted to meet the unique needs of pregnancy (DBT-P). The goal of this work is to improve perinatal mental health trajectories.

The premise of this study-that improving emotion regulation in pregnancy may disrupt intergenerational transmission of psychopathology-is informed by our research over the past two decades, including several NIH awards (R01MH119070, R01MH132210, R01DA049755, R21MH1090777, F31MH074196). The investigator' data reveal that maternal emotion dysregulation confers risk for mother. The research also shows that resting respiratory sinus arrhythmia (RSA), a physiological index of emotion dysregulation, can be improved via intervention in non-pregnant adults. The investigators propose that DBT-P will increase emotion regulation skills use or increase RSA in the mother (target engagement) leading to significant reductions in her emotion dysregulation prior to birth.

The primary study objectives are to recruit 100 pregnant women with high emotion dysregulation to receive either: (1) dialectical behavior therapy skills groups or an Assessment only control; and (2) to evaluate whether the treatment improved emotion regulation skills use as well as respiratory sinus arrhythmia.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
Female
Target Recruitment
100
Inclusion Criteria
  • Emotion dysregulation score of 88 or above
  • At least 12 weeks pregnant
  • Singleton Pregnancy
  • Fluent in English
Exclusion Criteria
  • Active psychosis
  • Drug or alcohol use disorder during pregnancy
  • High risk of an imminent suicide attempt
  • Significant health complications (e.g., cancer)
  • Illiterate and/or unable to independently complete and comprehend written measures

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Difficulties in Emotion Regulation Scale (DERS)Baseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

The DERS is a 36-item measure scored on a 5-point Likert Scale. DERS scores range from 36-180 and enrollment in this study requires a baseline total DERS score of ≥88 which indicate greater difficulties in emotion regulation.

Respiratory Sinus Arrhythmia (RSA)Baseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

RSA is a peripheral index of parasympathetic nervous system influences on cardiac activity and is measured as the variability in heart rate that coincides with respiration.

Secondary Outcome Measures
NameTimeMethod
Recruitment ratesBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility of the intervention will be assessed by evaluating recruitment rates.

Intervention adherenceBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility of the intervention will be assessed by evaluating intervention adherence. Weekly assessment of intervention adherence conducted by clinicians based on subject completion of required homework assignments, daily diary entries and group session attendance.

Number of women who complete all sessionsBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility will be assessed by how many women completed all sessions.

Number of interventionists who can self-monitor for fidelity, assessed by watching segments of video-recorded sessionsBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility will be assessed by whether the interventionist can self-monitor for fidelity.

Participation ratesPost-treatment (Week 10)

Acceptability will be assessed by participation rates.

Participant satisfaction with the intervention assessed by the Client Satisfaction QuestionnairePost-treatment (Week 10)

Acceptability will be assessed by measuring participant satisfaction with the intervention (including completion of the intervention) using the Client Satisfaction Questionnaire. Scores are summed across items once. Items 2, 4, 5, and 8 are reverse scored. Total scores range from 8 to 32, with the higher number indicating greater satisfaction.

Percent of missing dataBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility of the assessment schedule will include the percent of missing data at all time points.

Reasons for refusalBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility of the intervention will be assessed by evaluating reasons for refusal. Collection of reasons for refusal to be obtained via subject self-report at each individual timepoint; expected attendance for 85% of sessions.

Percent of participationBaseline (Week 0), mid-treatment (Week 5), and post-treatment (Week 10)

Feasibility of the assessment schedule will include the percent of participation at all timepoints.

Telehealth acceptability specific to DBT skills trainingPost-treatment (Week 10)

A 41-item original survey developed by DBT experts in the United States and Australia to measure participants' satisfaction with DBT delivered through telehealth. Items designed to assess relevance of care experience on a 5-pt scale from Not Relevant to Very Relevant. Responses anonymized and qualitative free-text fields provided for recommendations and comments for changes or improvements.

Trial Locations

Locations (1)

Duke University

🇺🇸

Durham, North Carolina, United States

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