Език: EN EN
← Назад към резултатите
Набира участници Не е приложимо NCT07016009

Thrive Person-Centered Planning Program for Young Adults With Fetal Alcohol Spectrum Disorders

Не е приложима фаза (напр. обсервационно)
Заболявания: Fetal Alcohol Spectrum Disorders

Спонсор: University of Rochester

Налично на: БГ
Обобщение
This study evaluates the Thrive person centered planning program for young adults with fetal alcohol spectrum disorders. Participants are randomized to either an immediate start or delayed start group for the psychoeducation phase. Following this phase, participants are randomized again to receive the intervention in either an individual or group based format. Participants complete repeated online assessments at multiple timepoints over approximately 10 months to evaluate whether the program improves goal setting, social support, and quality of life.
Описание
This study is a randomized, multi stage trial with two sequential randomization timepoints. At baseline, participants are randomized to either an immediate start psychoeducation group or a delayed start group. After completion of the psychoeducation phase, participants undergo a second randomization to receive the intervention in either an individual or group based goal setting format. This results in four study arms representing combinations of intervention timing and delivery format. Participants complete repeated assessments at multiple timepoints over approximately 10 months to evaluate effectiveness, goal setting format differences, and maintenance of outcomes.
Кой може да участва
Inclusion Criteria: * Young adult between the ages of 18 and 25 * Lives in the United States * Has a diagnosis of fetal alcohol spectrum disorder or confirmed prenatal alcohol exposure Exclusion Criteria: * Does not have access to the internet or data plan allowing video conferencing * Is not able to listen or speak in English
Интервенции
Thrive Program
BEHAVIORAL
Места на провеждане 1
САЩ (1)
University of Rochester
Rochester , New York
Технически детайли
Статус
Набира участници
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Максимална възраст
25 Years
Здрави доброволци
Не
Начална дата
14.04.2026
Крайна дата
31.08.2028
Регистрационен номер
NCT07016009
Източник
clinicaltrials.gov
Запитване за медицински туризъм

Информацията е извлечена автоматично от ClinicalTrials.gov. Консултирайте се с вашия лекар преди да предприемете действия.