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Study identifier: NCT06703242 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pilot Study on a Health Promotion Intervention for Ultra-Orthodox Mothers of Children With ADHD

Condition: Attention Deficit Disorder With Hyperactivity (ADHD)  ·  Sponsor: Adina Maeir

PhaseNA
Planned participants32
Who can joinFemale, N/A to no upper limit
Healthy volunteersYes

About this study

The goal of this study is to evaluate the feasibility and effectiveness of a health promotion intervention for Ultra-Orthodox Jewish mothers of children with ADHD. This study will examine the impact of a culturally tailored group-based intervention aimed at reducing stress, enhancing health, and improving the well-being of mothers. The main questions this study aims to answer are: 1. Is the intervention feasible for mothers to participate? 2. Does the intervention improve maternal knowledge about ADHD and reduce stigma? 3. Does it help reduce maternal stress and enhance self-care practices? Participants include: Mothers: Ultra-Orthodox Jewish mothers with a child (ages 6-12) diagnosed with ADHD and no other major health conditions in the family (other than ADHD). Educators: School educators with at least 5 years of experience teaching children with ADHD in the Ultra-Orthodox community. What participation involves: Mothers will attend six weekly teletherapy group sessions, with 6-8 mothers per group. They will complete questionnaires before and after the intervention (approximately 30 minutes each) and participate in a 90-minute remote focus group to provide feedback on the program. Educators will attend a single teletherapy group session (90 minutes) during the program (session 5) and participate in a 90-minute remote interview to provide feedback on the program.

This description comes directly from the study's public registry record.

Talk to the study team

Jennifer Budman, PhD  ·  972 503422600  ·  jennifer.budman@mail.huji.ac.il

Always discuss trial participation with your own doctor first.

Locations (1)

Hebrew UniversityJerusalem, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06703242