TY - JOUR
T1 - Wellbeing measurement among adults with Charcot-Marie-Tooth disease
AU - Rule, Payton D.
AU - Wolk, Megan W.
AU - Hill, Patrick L.
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/1
Y1 - 2024/1
N2 - Background and aims: Wellbeing research among individuals with Charcot-Marie-Tooth disease (CMT) is limited. The goal of the current study is to characterize the challenges experienced by adults with CMT that researchers may miss by utilizing typical strategies to capture mental health and wellbeing. Methods: In 2021, we recruited 288 US adults with CMT (MAge = 60 years, 59% Female, 93% White) to take part in an online survey. Participants were presented with validated wellbeing and health measures, in addition to newly created measures specific to CMT, and then asked to provide free-response feedback about aspects of their lived experiences missing from these measures. Thematic analysis were applied to the free-response data to identify CMT-related difficulties that may impact wellbeing among adults with CMT. Results: Results identified nine CMT-related challenges that are important to individuals with CMT and are often left out of wellbeing assessments in this population. The three most common themes identified were anxiety or worry, coping with loss of function or progression, and difficulty finding knowledgeable medical providers. Further, some aspects of the CMT experience may be comorbid. Interpretation: These results can be used to inform future research and clinical practice in the CMT population.
AB - Background and aims: Wellbeing research among individuals with Charcot-Marie-Tooth disease (CMT) is limited. The goal of the current study is to characterize the challenges experienced by adults with CMT that researchers may miss by utilizing typical strategies to capture mental health and wellbeing. Methods: In 2021, we recruited 288 US adults with CMT (MAge = 60 years, 59% Female, 93% White) to take part in an online survey. Participants were presented with validated wellbeing and health measures, in addition to newly created measures specific to CMT, and then asked to provide free-response feedback about aspects of their lived experiences missing from these measures. Thematic analysis were applied to the free-response data to identify CMT-related difficulties that may impact wellbeing among adults with CMT. Results: Results identified nine CMT-related challenges that are important to individuals with CMT and are often left out of wellbeing assessments in this population. The three most common themes identified were anxiety or worry, coping with loss of function or progression, and difficulty finding knowledgeable medical providers. Further, some aspects of the CMT experience may be comorbid. Interpretation: These results can be used to inform future research and clinical practice in the CMT population.
KW - Disabilities
KW - Inherited peripheral neuropathy
KW - Lived experience
KW - Wellbeing
UR - http://www.scopus.com/inward/record.url?scp=85218815372&partnerID=8YFLogxK
U2 - 10.1016/j.hctj.2024.100053
DO - 10.1016/j.hctj.2024.100053
M3 - Article
C2 - 39712593
AN - SCOPUS:85218815372
SN - 2949-9232
VL - 2
JO - Health Care Transitions
JF - Health Care Transitions
M1 - 100053
ER -