Variability in engagement and progress in efficacious integrated collaborative care for primary care patients with obesity and depression: Within-treatment analysis in the RAINBOW trial.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2020
2020
Historique:
received:
28
05
2019
accepted:
27
03
2020
entrez:
22
4
2020
pubmed:
22
4
2020
medline:
21
7
2020
Statut:
epublish
Résumé
The RAINBOW randomized clinical trial validated the efficacy of an integrated collaborative care intervention for obesity and depression in primary care, although the effect was modest. To inform intervention optimization, this study investigated within-treatment variability in participant engagement and progress. Data were collected in 2014-2017 and analyzed post hoc in 2018. Cluster analysis evaluated patterns of change in weekly self-monitored weight from week 6 up to week 52 and depression scores on the Patient Health Questionnaire-9 (PHQ-9) from up to 15 individual sessions during the 12-month intervention. Chi-square tests and ANOVA compared weight loss and depression outcomes objectively measured by blinded assessors to validate differences among categories of treatment engagement and progress defined based on cluster analysis results. Among 204 intervention participants (50.9 [SD, 12.2] years, 71% female, 72% non-Hispanic White, BMI 36.7 [6.9], PHQ-9 14.1 [3.2]), 31% (n = 63) had poor engagement, on average completing self-monitored weight in <3 of 46 weeks and <5 of 15 sessions. Among them, 50 (79%) discontinued the intervention by session 6 (week 8). Engaged participants (n = 141; 69%) self-monitored weight for 11-22 weeks, attended almost all 15 sessions, but showed variable treatment progress based on patterns of change in self-monitored weight and PHQ-9 scores over 12 months. Three patterns of weight change (%) represented minimal weight loss (n = 50, linear β1 = -0.06, quadratic β2 = 0.001), moderate weight loss (n = 61, β1 = -0.28, β2 = 0.002), and substantial weight loss (n = 12, β1 = -0.53, β2 = 0.005). Three patterns of change in PHQ-9 scores represented moderate depression without treatment progress (n = 40, intercept β0 = 11.05, β1 = -0.11, β2 = 0.002), moderate depression with treatment progress (n = 20, β0 = 12.90, β1 = -0.42, β2 = 0.006), and milder depression with treatment progress (n = 81, β0 = 7.41, β1 = -0.23, β2 = 0.003). The patterns diverged within 6-8 weeks and persisted throughout the intervention. Objectively measured weight loss and depression outcomes were significantly worse among participants with poor engagement or poor progress on either weight or PHQ-9 than those showing progress on both. Participants demonstrating poor engagement or poor progress could be identified early during the intervention and were more likely to fail treatment at the end of the intervention. This insight could inform individualized and timely optimization to enhance treatment efficacy. ClinicalTrials.gov# NCT02246413.
Identifiants
pubmed: 32315362
doi: 10.1371/journal.pone.0231743
pii: PONE-D-19-15164
pmc: PMC7173791
doi:
Banques de données
ClinicalTrials.gov
['NCT02246413']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0231743Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL119453
Pays : United States
Commentaires et corrections
Type : ErratumIn
Déclaration de conflit d'intérêts
The authors declare that no competing interests existed for the research as reported. Dr. Lenard Lesser’s affiliation with 1Life Healthcare/One Medical constituted no competing interests. Dr. Lesser had originally supported on the NIH grant for his role as a study physician on this study while he was an employee at the Palo Alto Medical Foundation Research Institute (PAMFRI) where the study was conducted. Starting from 07/2016 till 10/2017, Dr. Lesser transitioned from PAMFRI to 1Life Healthcare, Inc/One Medical. At that time, his continuous involvement in the study was compensated through a research contract as an independent consultant with PAMFRI specifically for the NIH grant supporting the study. 1Life Healthcare/One Medical provided no support of any form for the study; and had no role in the study design, data collection/analysis, decision to publish, or preparation of the manuscript. This does not alter our adherence to PLOS ONE policies on sharing data and materials.”
Références
NCHS Data Brief. 2014 Oct;(167):1-8
pubmed: 25321386
J Psychiatr Res. 2010 Nov;44(15):1043-51
pubmed: 20537350
JAMA. 2019 Mar 5;321(9):869-879
pubmed: 30835308
Obesity (Silver Spring). 2017 Dec;25(12):2062-2067
pubmed: 29086487
Psychol Med. 2010 Aug;40(8):1367-77
pubmed: 19863842
Obesity (Silver Spring). 2014 Jul;22(7):1608-16
pubmed: 24771618
JAMA. 2018 Apr 24;319(16):1723-1725
pubmed: 29570750
J Affect Disord. 2011 Mar;129(1-3):126-42
pubmed: 20926139
Int J Obes (Lond). 2013 Nov;37(11):1427-34
pubmed: 23459323
Obesity (Silver Spring). 2015 Jul;23(7):1353-6
pubmed: 26110890
J Gen Intern Med. 2001 Sep;16(9):606-13
pubmed: 11556941
Epilepsy Behav. 2010 Nov;19(3):225-31
pubmed: 20609631
Ann Behav Med. 2011 Feb;41(1):119-30
pubmed: 20878292
J Health Psychol. 2008 Nov;13(8):1190-7
pubmed: 18987092
Arch Gen Psychiatry. 2010 Mar;67(3):220-9
pubmed: 20194822
J Affect Disord. 2015 Feb 1;172:274-90
pubmed: 25451427
JAMA Intern Med. 2013 Jan 28;173(2):113-21
pubmed: 23229846
BMC Fam Pract. 2009 Nov 12;10:71
pubmed: 19909549
JAMA. 2018 Sep 18;320(11):1172-1191
pubmed: 30326501
Am J Prev Med. 2009 Dec;37(6):505-11
pubmed: 19944916
Br J Psychiatry. 1976 Jul;129:61-7
pubmed: 938806
Contemp Clin Trials. 2015 Jul;43:260-78
pubmed: 26096714
Obesity (Silver Spring). 2014 Jan;22(1):45-51
pubmed: 23740619
BMC Psychiatry. 2012 Oct 30;12:181
pubmed: 23110575
J Affect Disord. 2016 May;195:119-26
pubmed: 26890289
Med Care. 2018 Aug;56(8):719-726
pubmed: 29939912
Multivariate Behav Res. 2015;50(1):91-108
pubmed: 26609745
CMAJ Open. 2014 Oct 01;2(4):E306-17
pubmed: 25485258
J Clin Psychopharmacol. 2005 Aug;25(4 Suppl 1):S8-13
pubmed: 16027561
Int J Obes (Lond). 2015 Oct;39(10):1558-60
pubmed: 25982792
Arch Gen Psychiatry. 1978 Oct;35(10):1189-95
pubmed: 697537
PLoS One. 2018 Sep 7;13(9):e0202245
pubmed: 30192786
N Engl J Med. 2010 Dec 30;363(27):2611-20
pubmed: 21190455
PLoS One. 2014 Sep 29;9(9):e108114
pubmed: 25264616
J Psychosom Res. 2014 Oct;77(4):247-63
pubmed: 25201482
JAMA. 2004 Apr 7;291(13):1569-77
pubmed: 15069044
Arch Intern Med. 2006 Nov 27;166(21):2314-21
pubmed: 17130383
BMC Psychiatry. 2013 Sep 12;13:223
pubmed: 24028572
N Engl J Med. 2002 Feb 7;346(6):393-403
pubmed: 11832527
Value Health. 2016 Jul-Aug;19(5):602-13
pubmed: 27565277