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N/A N=41 Randomized Prevention

A Substance Use Adaptation of Fathering Through Change

Parenting · Substance Use

Enrolled (actual)
41
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: TOPSE: Group Mean Change at 6 Weeks and 4 Months on the Tool of Parenting Self-Efficacy — 8.77; 7.50; 8.70; 7.65 score on a scale — p=0.014

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Fathering Through Change (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
University of Oregon
Primary completion
Dec 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
TOPSE: Group Mean Change at 6 Weeks and 4 Months on the Tool of Parenting Self-Efficacy
8.77; 7.50; 8.70; 7.65 0.014 sig
PRIMARY
PPI Harsh: Group Mean Change at 6 Weeks and 4 Months the Parenting Practices Interview Harsh Parenting Subscale
1.67; 2.08; 1.83; 2.00 0.80
PRIMARY
PPI Inept: Group Mean Change at 6 Weeks and 4 Months the Parenting Practices Interview Inept Parenting Subscale
2.09; 2.91; 2.09; 2.64 0.009 sig
PRIMARY
PPI Prosocial: Group Mean Change at 6 Weeks and 4 Months the Parenting Practices Interview Prosocial Parenting Subscale
5.07; 4.33; 4.93; 4.80 0.118
SECONDARY
Substance Use: Group Mean Change at 6 Weeks and 4 Months on Any Use in the Last 30 Days
4; 6; 4; 8 .24
SECONDARY
Substance Use: Group Mean Change at 6 Weeks and 4 Months on Days of Use the Last 30
0; 0; 0; 0 0.43
SECONDARY
SDQ: Group Mean Change at 4 Months on Child Behavior
9; 16 0.07

Summary

This study is a randomized control trial of the Fathering Through Change intervention, delivered via text messaging, to fathers in recovery for substance use disorders.

Eligibility Criteria

Inclusion Criteria

  • identify as being in recovery
  • abstinent from illicit substances for at least 1 day and less than one year at time of enrollment
  • parenting responsibilities for a child between the ages of 3-16
  • spend at least 2 hours per week with child between ages of 3-16
  • English speaking

Exclusion Criteria

-

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04532619). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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