Evidence map›Paper›PMID 39134393›Full record

ArticleJournal of intellectual disability research : JIDR2024

Description and predictors of self-determination in males and females with fragile X syndrome on the verge of adulthood.

L Friedman, C Moser, A J Thurman, J L Taylor, L Abbeduto, J Klusek

Abstract read
In one paragraph

Article in Journal of intellectual disability research : JIDR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

L FriedmanDepartment of Communication Sciences and Disorders, University of South Carolina, Columbia, SC, USA.ORCID 0000-0001-7279-0820
C MoserDepartment of Communication Sciences and Disorders, University of South Carolina, Columbia, SC, USA.ORCID 0000-0002-1903-4345
A J ThurmanDepartment of Psychiatry and Behavioral Sciences and MIND Institute, University of California Davis Health, Sacramento, CA, USA.
J L TaylorDepartment of General Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
L AbbedutoDepartment of Psychiatry and Behavioral Sciences and MIND Institute, University of California Davis Health, Sacramento, CA, USA.
J KlusekDepartment of Communication Sciences and Disorders, University of South Carolina, Columbia, SC, USA.

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Preclinical CoreP50HD103573 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI GABRIEL S DICHTER · 2020 to 2026
$9.7M
Research Project: Pathologic Significance of Maternal AutoantibodiesP50HD103526 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEONARD J. ABBEDUTO, Melissa Dawn Bauman · 2020 to 2026
$9.7M
LINGUISTIC COMMUNICATION AND MENTAL RETARDATIONR01HD024356 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI ABBEDUTO, LEONARD J. · 1987 to 2022
$9.0M
Aging Symptom Trajectories in Mother Carriers of the FMR1 PremutationR01AG073374 · NIA · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI Jessica Klusek · 2022 to 2026
$3.4M
Defining the Language Phenotype of the FMR1 PremutationR21DC017804 · NIDCD · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI KLUSEK, JESSICA · 2019 to 2021
$684k
Neuropsychological Profiles and Risk for Dementia-Related Disease in Mothers of Children with Autism Spectrum DisorderF32AG079615 · NIA · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FRIEDMAN, LAURA ANNE · 2022 to 2024
$223k
National Institute of Child Health and Human Development P50HD103526National Institute of Child Health and Human Development R01HD024356NIA NIH HHS F32 AG079615NIA NIH HHS F32AG079615NIA NIH HHS R01 AG073374NIA NIH HHS R01AG073374NICHD NIH HHS P50 HD103526NICHD NIH HHS P50 HD103537NICHD NIH HHS P50 HD103573NICHD NIH HHS R01 HD024356NIDCD NIH HHS R21 DC017804NIDCD NIH HHS R21DC017804Research Participant Registry Core of the Carolina Institute for Developmental Disabilities P50HD103573
6 · The paper itself

Abstract

backgroundSelf-determination refers to setting goals and making decisions regarding one's own life with support from others as needed. Research on people with intellectual and developmental disabilities has established the importance of self-determination for quality of life outcomes, such as increased independence and life satisfaction. However, self-determination has not been characterised specifically in fragile X syndrome (FXS), the leading inherited cause of intellectual disability. Relative to youth with other forms of intellectual and developmental disabilities, youth with FXS may face exceptional barriers to the development of self-determined behaviour. In addition to intellectual disability, the FXS behavioural profile is characterised by high rates of autism and anxiety that may further limit opportunities for youth with FXS. The heritable nature of the condition can also yield a distinctive family environment, with siblings and parents also living with fragile X or its associated conditions. Considering these unique challenges, the present study examined self-determination in young adult males and females with FXS and explored whether factors such as language skills, adaptive behaviour and autism traits were associated with self-determination capacity and opportunities.

methodsThe present study included 9 females and 36 males with FXS between the ages of 17 and 25 years. Caregivers (mothers or fathers) completed the American Institute for Research Self-Determination Assessment, which is a questionnaire that yields three scores: self-determination capacity, opportunities for self-determination at home and opportunities for self-determination at school.

resultsCaregivers endorsed a wide range of self-determination capacity and opportunities, with ratings for opportunities at home and school exceeding ratings of capacity. Better adaptive behaviour skills were associated with more self-determination capacity, and the presence of more autism traits was associated with fewer opportunities at school.

conclusionsResults from this study contribute to our understanding of avenues to best support young adults with FXS as they transition to adulthood. Our findings also have implications for practice, such that interventions targeting adaptive behaviours and self-determination may be an effective approach for promoting autonomy and independence for young adults with FXS. Additionally, caregivers and educators should continue to provide opportunities to practise self-determination, regardless of their perception of capacity.

Indexed as

Fragile X SyndromePersonal AutonomyAdolescentAdultFemaleHumansMaleYoung AdultautismFMR1fragile X syndromeintellectual disabilityself‐determinationtransition to adulthood

Identifiers

PMID39134393
PMCPMC11881981

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.