TY - JOUR
T1 - Digital cognitive behavioral therapy vs education for pain in adults with sickle cell disease
AU - Jonassaint, Charles R.
AU - Lalama, Christina M.
AU - Carroll, C. Patrick
AU - Badawy, Sherif M.
AU - Hamm, Megan E.
AU - Stinson, Jennifer N.
AU - Lalloo, Chitra
AU - Saraf, Santosh L.
AU - Gordeuk, Victor R.
AU - Cronin, Robert M.
AU - Shah, Nirmish
AU - Lanzkron, Sophie M.
AU - Liles, Darla
AU - O’Brien, Julia A.
AU - Trimnell, Cassandra
AU - Bailey, Lakiea
AU - Lawrence, Raymona H.
AU - Jean, Leshana Saint
AU - DeBaun, Michael
AU - De Castro, Laura M.
AU - Palermo, Tonya M.
AU - Abebe, Kaleab Z.
N1 - © 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.
PY - 2024/10/7
Y1 - 2024/10/7
N2 - Despite the burden of chronic pain in sickle cell disease (SCD), nonpharmacological approaches remain limited. This multisite, randomized trial compared digital cognitive behavioral therapy (CBT) with a digital pain/SCD education program (“Education”) for managing pain and related symptoms. Participants were recruited virtually from seven SCD centers and community organizations in the United States. Adults (aged ≥18 years) with SCD-related chronic pain and/or daily opioid use were assigned to receive either CBT or Education for 12 weeks. Both groups used an app with interactive chatbot lessons and received personalized health coach support. The primary outcome was the change in pain interference at six months, with secondary outcomes including pain intensity, depression, anxiety, quality of life, and self-efficacy. Of 453 screened participants, 359 (79%) were randomized to CBT (n = 181) or Education (n = 178); 92% were Black African American, and 66.3% were female. At six months, 250 participants (70%) completed follow-up assessments, with 16 (4%) withdrawals. Engagement with the chatbot varied, with 76% connecting and 48% completing at least one lesson, but 80% of participants completed at least one health coach session. Both groups showed significant within-group improvements in pain interference (CBT: −2.13; Education: −2.66), but no significant difference was observed between them (mean difference, 0.54; P = .57). There were no between-group differences in pain intensity, depression, anxiety, or quality of life. High engagement with health coaching and variable engagement with digital components may explain the similar outcomes between interventions in this diverse, hard-to-reach population.
AB - Despite the burden of chronic pain in sickle cell disease (SCD), nonpharmacological approaches remain limited. This multisite, randomized trial compared digital cognitive behavioral therapy (CBT) with a digital pain/SCD education program (“Education”) for managing pain and related symptoms. Participants were recruited virtually from seven SCD centers and community organizations in the United States. Adults (aged ≥18 years) with SCD-related chronic pain and/or daily opioid use were assigned to receive either CBT or Education for 12 weeks. Both groups used an app with interactive chatbot lessons and received personalized health coach support. The primary outcome was the change in pain interference at six months, with secondary outcomes including pain intensity, depression, anxiety, quality of life, and self-efficacy. Of 453 screened participants, 359 (79%) were randomized to CBT (n = 181) or Education (n = 178); 92% were Black African American, and 66.3% were female. At six months, 250 participants (70%) completed follow-up assessments, with 16 (4%) withdrawals. Engagement with the chatbot varied, with 76% connecting and 48% completing at least one lesson, but 80% of participants completed at least one health coach session. Both groups showed significant within-group improvements in pain interference (CBT: −2.13; Education: −2.66), but no significant difference was observed between them (mean difference, 0.54; P = .57). There were no between-group differences in pain intensity, depression, anxiety, or quality of life. High engagement with health coaching and variable engagement with digital components may explain the similar outcomes between interventions in this diverse, hard-to-reach population.
KW - Adult
KW - Anemia, Sickle Cell/therapy
KW - Chronic Pain/therapy
KW - Cognitive Behavioral Therapy/methods
KW - Female
KW - Humans
KW - Male
KW - Middle Aged
KW - Pain Management/methods
KW - Patient Education as Topic
KW - Quality of Life
KW - Treatment Outcome
UR - http://www.scopus.com/inward/record.url?scp=85213277074&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2024013861
DO - 10.1182/bloodadvances.2024013861
M3 - Article
C2 - 39374587
AN - SCOPUS:85213277074
SN - 2473-9529
VL - 8
SP - 6257
EP - 6266
JO - Blood Advances
JF - Blood Advances
IS - 24
ER -