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Feasibility of the 5-Step Method in the U.S.

A Feasibility Study of Delivery of the 5-Step Method Intervention for Family Members of Persons With Substance Use Disorder in the United States

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06565429
Enrollment
24
Registered
2024-08-22
Start date
2024-09-01
Completion date
2026-08-06
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol-Related Disorders, Coping Skills, Family Members, Relatives, Stress Physiology, Stress, Psychological, Substance-Related Disorders

Keywords

Social Support

Brief summary

The purpose of this study is to see if it is possible (feasible) to introduce a behavioral intervention for family members affected by a relative's misuse of drugs and/or alcohol in the United States. The intervention is called the 5-Step Method. It will be a randomized control trial, with a total of 24 participants, and 12 in each group. The study lasts for approximately 12 weeks for the participant. The intervention group will receive a self-help handbook of the 5-Step Method, and the control group will not. Although the control group will not receive an intervention from the research team, they are allowed to look for and use any currently available program for affected family members (for example, Al-Anon, or Nar-Anon) during the study period. The study is being done because the 5-Step Method has not been used or evaluated in the U.S. (or the creators are unaware that it is in use here). There are two aims (objectives): (1) to see if it is feasible to introduce the 5-Step Method into the U.S.; (2) to look at trends in the baseline and followup survey scores to see if there is evidence of preliminary participant response.

Detailed description

The study will be implemented in the United States using online contacts via Zoom and email. A participant in the study will be an affected family member of someone with drug and/or alcohol misuse who has been experiencing stress as a result of the substance misuse for at least the past six months. Both stress and their relative's misuse will be self-identified by the participant. A participant will reside in the United States of America. Recruitment for the study will include advertisements via social media, newspaper notices, and flyers posted at stores and healthcare sites. Once potential participants have contacted the PI and have been screened, consented, and have completed the baseline survey, they will be randomized into either the intervention group or the control group. Once randomized the participant and PI will no longer be blinded to the treatment condition. Those in the intervention group will receive the self-help handbook via the U.S. mail. The control group does not receive an intervention, but could use currently available programs if desired, although information about these programs will not be provided by the PI. All participants will receive emails at regular intervals during their 12-week study period. Because the intervention is completed at the individual level, study recruitment will occur on a rolling basis until 24 participants have been enrolled. Data regarding the feasibility of the study (recruitment, retention, refusal rates, etc.) will be collected. Baseline and follow up surveys will be compared for evidence of participant response.

Interventions

BEHAVIORAL5-Step Method Intervention

The 5-Step Method (5SM) intervention is delivered through a self-help handbook: There are writing prompts for the affected family member (AFM) in each step. The steps end with a summary, a space to reflect and a statement that the step is complete but can be reviewed as needed. The steps are: 1.Explore how the relative's drug and/or alcohol misuse is affecting the family member, causing stress and strain. 2.Determine the information the AFM needs to understand the situation using evidence-based websites in the handbook. 3.Reflect on coping styles, and which ones might be useful. 4.Determine who is a source of positive social support, and who could be one that the AFM has not used yet. 5.Review steps 1-4 and determine if the AFM is feeling less stress and strain, or if more help is needed and use websites to look for additional help. The activities should take about 1 hour per week.

Sponsors

Villanova University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* at least 18 years old * able to read, write, speak, and understand English * live in the United States of America * be a family member who self-reports stress/strain because of a relative's drug and/or alcohol misuse * have access to the Internet and a smartphone or larger device to complete study surveys * have a personal email address they do not share with others that can receive study related emails * have the ability to freely consent to participate in the study based on their understanding

Exclusion criteria

-if person states the relative with alcohol and/or drug misuse has been physically violent towards the potential participant

Design outcomes

Primary

MeasureTime frameDescription
AcceptabilityOne year post completing the interventionScores on Acceptability of Intervention Measure (Weiner et al., 2017), a validated and standardized instrument combined with eight other acceptability questions specific to the 5-Step Method Handbook.
Study process ratesOne year post completing the intervention. Rates will be tallied at the end of the studyStudy process rates will be assessed by quantitatively tracking the recruitment rate, retention rate, refusal rate, eligibility rate, and study completion rate.
Likelihood of adverse eventsOne year post completing the interventionSafety will be assessed for all participants by quantitatively summarizing the number of adverse events that are considered to be unexpected, serious, and/or possibly or definitely related to the study
ResourcesOne year post completing the interventionHow much time all individual participants spent filling out the surveys, assessed via a survey
Adherence to treatment protocol12 weeks after starting study, if placed in the intervention groupThe adherence to treatment protocol will be assessed by asking the intervention group questions about how they interacted with the self-help handbook to determine if they used the handbook as designed or if they used it in some other way.
MarketingOne year post completing the intervention. Will review responses and tally resultsMarketing of the study will be assessed by asking those who inquire about the study where they learned about the study to determine which locations may be better for recruitment in future studies.
Ease of useOne year post completing the interventionEase of use of the study will be assessed by asking participants two questions at the end of the follow-up survey about the way the surveys were worded. The answers of these questions will be reviewed and tallied as well as qualitatively described. The surveys of the study are validated tools, and the only allowed changes to the survey questions were to change from UK English to US English on spelling alone (behaviour to behavior for example). Syntax and word choice were not allowed to be changed. It is possible that how the phrases are stated and the words used will not be as easy to read for an American as compared to someone from the UK, where the intervention was created. The two questions ask if there were any difficulties understanding the survey, and if so, did they think this may have affected how they answered any of the questions.

Secondary

MeasureTime frameDescription
StressBaseline and change over 12 week periodFamily Member Impact Questionnaire (FMI) Scores range from 0-48, with higher scores indicating higher stress.
CopingBaseline and change over 12 week periodSymptom Rating Test (SRT) Scores range from 0-90. There are three subscales of coping, with higher scores on two subscales generally associated with higher scores on stress and strain. One subscale is generally associated with lower scores on stress and strain.
StrainBaseline and change over 12 week periodCoping Questionnaire (CQ) Scores range from 0-60, higher scores indicating higher scores higher strain.
Social SupportBaseline and change over 12 week periodAlcohol, Drugs, and the Family Social Support Scale (ADF-SSS) Scores range from 0-75 for the total score. Two subscales with higher scores show improved social support, while the third subscale should have lower numbers when there is an improvement.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORTherese M Collins, MS, RN

Villanova University

PRINCIPAL_INVESTIGATORHelene Moriarty, PhD, RN, FAAN

Villanova University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026