NCT07529548 · Charla Aubrey Rhodes
The New Beginnings Podcast: Brief Audio Intervention for Parents From Divorced and Separated Families
(NBP-P)
What this study is about
The goal of this study is to learn if the New Beginnings Podcast can help children whose parents are going through a divorce or separation. The podcast shares parenting strategies that have been shown to help in past in-person and online programs. This study will also look at how easy it is for parents to use the podcast and how helpful they find it. The main questions it aims to answer are: 1.
View original scientific description
The goal of this study is to learn if the New Beginnings Podcast can help children whose parents are going through a divorce or separation. The podcast shares parenting strategies that have been shown to help in past in-person and online programs. This study will also look at how easy it is for parents to use the podcast and how helpful they find it. The main questions it aims to answer are: 1. Do parents find the podcast easy to use, helpful, and relevant? 2. Does listening to the podcast improve children's mental health? 3. Does the podcast help parents build stronger relationships with their children and reduce conflict between parents? Researchers will compare families who use the podcast to families on a waitlist to see if the podcast makes a difference. Participants will: 1. Listen to podcast episodes over the course of the study 2. Answer questions about their experiences with the podcast 3. Complete surveys about their child's well-being, their parenting, and family relationships This study will include 80 parents and their children.
Interventions
BEHAVIORAL
New Beginnings Podcast Program
Parents will listen to 5 episodes of the New Beginnings Podcast (NBP-P) over 5 weeks. They will listen to one episode per week.
OTHER
No Interventions
Parents in the waitlist group will get access to the podcast after completion of the post-test survey or withdrawal from the study.
Primary outcome measures
Feasibility of Intervention
Time frame: Collected at Post-test only (Week 7) for Intervention Group Only
Feasibility of Intervention Measure (FIM) The FIM assesses the extent to which an intervention can be successfully used or carried out in a given context or setting (Weiner et al., 2017). It includes 4 items rated on a 5-point Likert scale (1=Completely disagree to 5=Completely agree). Item responses are averaged (range 1-5); higher scores indicate greater perceived feasibility. Psychometric evaluation shows acceptable reliability and validity alongside AIM and IAM.
Usability of Intervention
Time frame: Collected at Post-test only (Week 7) for Intervention Group only
Intervention Usability Scale (IUS) Usability of the intervention will be assessed using the Intervention Usability Scale (IUS), a 10-item self-report questionnaire adapted from the System Usability Scale (SUS). Items are rated on a 5-point scale ranging from 0 to 4, with response options reflecting increasing agreement. Item scores span the full possible range (0-4). Item responses are averaged to compute a mean usability score (range 0-4), with higher scores indicating greater perceived usability. Emerging psychometrics support a two-factor structure ("Usable" and "Learnable") alongside a reliable total score (Lyon et al., 2021).
Acceptability of Intervention
Time frame: Collected at Post-test only (Week 7) for Intervention Group only
Acceptability of Intervention Measure (AIM) The AIM assesses perceived acceptability of an intervention among intended users/implementers (Weiner et al., 2017). It contains 4 items rated on a 5-point Likert scale (1=Completely disagree to 5=Completely agree). Scores are typically averaged (range 1-5), with higher values indicating greater acceptability. Initial development and testing demonstrated strong content validity, structural validity, reliability, known-groups validity, and responsiveness
Appropriateness of Intervention
Time frame: Collected at Post-test only (Week 7) for Intervention Group only
Intervention Appropriateness Measure (IAM) The IAM assesses perceived appropriateness or fit of an intervention for a given setting, provider role, or target population (Weiner et al., 2017). It includes 4 items rated on a 5-point Likert scale (1=Completely disagree to 5=Completely agree). Item responses are averaged to produce a 1-5 score; higher values indicate the intervention is viewed as a better fit. Development work shows sound psychometric properties consistent with AIM and FIM.
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- For Parents, eligibility criteria are:
- divorced, separated, separated but never married, or divorcing/separating within the last two years;
- one or more children between the ages of 8-18 years old;
- have in-person contact with their child(ren) at least three hours per week or have at least one overnight visit every other week;
- have access to a smartphone with internet that can play audio files;
- English speaking. For children, eligibility criteria are:
- have a parent who is participating in the trial;
- be between the ages of 8-18 and
- have access to a computer to complete assessments. If a parent has more than one child aged 8-18 interested in participating, we will randomly select one child to ensure independence of responses.
Where
- Tempe, Arizona
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Apr 14, 2026 · Source of record for eligibility and locations