- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT07856927
To Share or Not To Share: Navigating Disclosure and Stigma Among Family Caregivers of Autistic Young Adults_Group Intervention
This study is a caregiver support program for family caregivers of autistic young adults (ages 18 to 26) as their family members navigate young adulthood. The program includes six 60-minute virtual sessions focused on making sense of caregiving roles during young adulthood, reflecting on everyday family experiences, supporting decision-making within families, deciding when and how to share experiences with others, and thinking about the future.
Tutkimuksen yleiskatsaus
Yksityiskohtainen kuvaus
This program has three components:
- program participation, which includes six virtual sessions and one optional celebration session
- eight surveys, including one pre-program survey, one post-program survey, and six post-session surveys to collect participants feedback on each session; and
- one optional one-on-one interview.
For the six sessions, this program utilizes a peer-facilitated model, recognizing the unique expertise that comes from lived experience. Some aspects of navigating transition can only be fully understood and effectively communicated by fellow family caregivers, rather than by professionals.
Attendees are encouraged to bring their broader life experiences, including those unrelated to caregiving, when they see these experiences as central to who they are. The program welcomes participants as whole people, honoring both their caregiving role and the parts of their lives that extend beyond it.
Session content and topics are built from a series of interviews with family caregivers. The program not only covers what was openly discussed in those interviews but also explores what was less visible, what may have been unspoken, hidden, or missing from the conversations.
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Vaihe
- Ei sovellettavissa
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Sang Qin, PhD
- Sähköposti: sqin38@wisc.edu
Opiskelupaikat
-
-
Wisconsin
-
Madison, Wisconsin, Yhdysvallat, 53705
- Rekrytointi
- University of Wisconsin
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Lapsi
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
Inclusion Criteria:
- Has a family member aged 18-26 who has received an autism-related diagnosis from a healthcare professional
- Must be a primary caregiver for this family member
- Must be able to speak, understand, and read English well
- Participants will be able to provide consent themselves.
Exclusion Criteria:
- Lack of proficiency in English
- Not a primary caregiver for a family member with autism aged 18-26
- Individuals requiring a guardian to provide consent will be excluded
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Tukevaa hoitoa
- Jako: Ei käytössä
- Inventiomalli: Yksittäinen ryhmätehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: Family Caregivers
Family Caregivers of Autistic Young Adults |
Six 60-min virtual sessions Surveys before and after program intervention Optional post-intervention interview
Muut nimet:
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Devaluation of Consumer Families (DCFS) Scale
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
9-items scored on a 4 point likert scale from 1 (strongly disagree) to 4 (strongly agree). Total range of scores is 9-36 with higher scores indicating higher devaluation of the family. |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Self-Compassion Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Self-Compassion Scale (26-item), scored from 26 to 130, with higher scores indicating greater self-compassion. |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Caregiving Appraisal Scale Score: Agreement
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Caregiving Appraisal Scale (6-item) scored from 6-30 where higher scores indicate higher appraisal. |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Caregiving Appraisal Scale Score: Frequency
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Caregiving Appraisal Scale (23-item) scored from 23-115 where higher scores indicate more frequency of appraisal. |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Family Empowerment Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Family Empowerment Scale (12-item) scored from 12-60 with higher scores meaning more empowered. |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
State Hope Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
State Hope Scale (6-item) scored from 6-48 where higher scores indicate more hope |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Caregiving Confidence Scale (CSES-8) Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
CSES-8 scored from 1-10 with higher scores meaning more confidence |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Affiliate Stigma Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Affiliate Stigma Scale (22-item) scored from 22-88 where higher scores indicate increased stigma |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Caregiving Flexibility Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Caregiving flexibility score (18-item) scored from 18-72 where higher scores indicate increased flexibility |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Feeling of Loneliness Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Feeling of Loneliness (3-item) scored from 3-9 where higher scores indicate increased loneliness |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Autonomy Support Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Autonomy Support Scale (5-item) scored from 5-20 where higher scores indicate more autonomy |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
|
Emotional Support Scale Score
Aikaikkuna: baseline (pre-intervention) and 6 weeks (post-intervention)
|
Emotional Support Scale (6-item) scored from 6-30 where higher scores indicate increased emotional support |
baseline (pre-intervention) and 6 weeks (post-intervention)
|
Yhteistyökumppanit ja tutkijat
Sponsori
Tutkijat
- Päätutkija: Sang Qin, PhD, University of Wisconsin, Madison
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
Lisää tietoa
Tähän tutkimukseen liittyvät termit
Avainsanat
Muita asiaankuuluvia MeSH-ehtoja
Muut tutkimustunnusnumerot
- 2026-1026
- Protocol Version CP002 (Muu tunniste: UW Madison)
- SOE | Rehab Psy & Sp Ed Ops (Muu tunniste: UW Madison)
Yksittäisten osallistujien tietojen suunnitelma (IPD)
Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?
Lääke- ja laitetiedot, tutkimusasiakirjat
Tutkii yhdysvaltalaista FDA sääntelemää lääkevalmistetta
Tutkii yhdysvaltalaista FDA sääntelemää laitetuotetta
Nämä tiedot haettiin suoraan verkkosivustolta clinicaltrials.gov ilman muutoksia. Jos sinulla on pyyntöjä muuttaa, poistaa tai päivittää tutkimustietojasi, ota yhteyttä register@clinicaltrials.gov. Heti kun muutos on otettu käyttöön osoitteessa clinicaltrials.gov, se päivitetään automaattisesti myös verkkosivustollemme .