TY - JOUR
T1 - Sertraline for anxiety in adults with a diagnosis of autism (STRATA)
T2 - study protocol for a pragmatic, multicentre, double-blind, placebo-controlled randomised controlled trial
AU - on behalf of the STRATA autistic advisory group
AU - Rai, Dheeraj
AU - Webb, Doug
AU - Lewis, Amanda
AU - Cotton, Leonora
AU - Norris, Jade Eloise
AU - Alexander, Regi
AU - Baldwin, David S.
AU - Brugha, Traolach
AU - Cochrane, Madeleine
AU - Del Piccolo, Maria Chiara
AU - Glasson, Emma J.
AU - Hatch, Katherine K.
AU - Kessler, David
AU - Langdon, Peter E.
AU - Leonard, Helen
AU - MacNeill, Stephanie J.
AU - Mills, Nicola
AU - Morales, Maximiliano Vazquez
AU - Morgan, Zoe
AU - Mukherjee, Raja
AU - Realpe, Alba X.
AU - Russell, Ailsa
AU - Starkstein, Sergio
AU - Taylor, Jodi
AU - Turner, Nicholas
AU - Thorn, Joanna
AU - Welch, Jack
AU - Douglas, Sarah
AU - Hale, Peter
AU - O’Brien, Sarah
AU - Walker, Amy
AU - Wiles, Nicola
N1 - Publisher Copyright:
© 2024, The Author(s).
PY - 2024/12
Y1 - 2024/12
N2 - Background: Selective serotonin reuptake inhibitors (SSRIs) are commonly prescribed to manage anxiety in adults with an autism diagnosis. However, their effectiveness and adverse effect profile in the autistic population are not well known. This trial aims to determine the effectiveness and cost-effectiveness of the SSRI sertraline in reducing symptoms of anxiety and improving quality of life in adults with a diagnosis of autism compared with placebo and to quantify any adverse effects. Methods: STRATA is a two-parallel group, multi-centre, pragmatic, double-blind, randomised placebo-controlled trial with allocation at the level of the individual. It will be delivered through recruiting sites with autism services in 4 regional centres in the United Kingdom (UK) and 1 in Australia. Adults with an autism diagnosis and a Generalised Anxiety Disorder Assessment (GAD-7) score ≥ 10 at screening will be randomised 1:1 to either 25 mg sertraline or placebo, with subsequent flexible dose titration up to 200 mg. The primary outcome is GAD-7 scores at 16 weeks post-randomisation. Secondary outcomes include adverse effects, proportionate change in GAD-7 scores including 50% reduction, social anxiety, obsessive-compulsive symptoms, panic attacks, repetitive behaviours, meltdowns, depressive symptoms, composite depression and anxiety, functioning and disability and quality of life. Carer burden will be assessed in a linked carer sub-study. Outcome data will be collected using online/paper methods via video call, face-to-face or telephone according to participant preference at 16, 24 and 52 weeks post-randomisation, with brief safety checks and data collection at 1–2, 4, 8, 12 and 36 weeks. An economic evaluation to study the cost-effectiveness of sertraline vs placebo and a QuinteT Recruitment Intervention (QRI) to optimise recruitment and informed consent are embedded within the trial. Qualitative interviews at various times during the study will explore experiences of participating and taking the trial medication. Discussion: Results from this study should help autistic adults and their clinicians make evidence-based decisions on the use of sertraline for managing anxiety in this population. Trial registration: ISRCTN, ISRCTN15984604 . Registered on 08 February 2021. EudraCT 2019-004312-66. ANZCTR ACTRN12621000801819. Registered on 07 April 2021.
AB - Background: Selective serotonin reuptake inhibitors (SSRIs) are commonly prescribed to manage anxiety in adults with an autism diagnosis. However, their effectiveness and adverse effect profile in the autistic population are not well known. This trial aims to determine the effectiveness and cost-effectiveness of the SSRI sertraline in reducing symptoms of anxiety and improving quality of life in adults with a diagnosis of autism compared with placebo and to quantify any adverse effects. Methods: STRATA is a two-parallel group, multi-centre, pragmatic, double-blind, randomised placebo-controlled trial with allocation at the level of the individual. It will be delivered through recruiting sites with autism services in 4 regional centres in the United Kingdom (UK) and 1 in Australia. Adults with an autism diagnosis and a Generalised Anxiety Disorder Assessment (GAD-7) score ≥ 10 at screening will be randomised 1:1 to either 25 mg sertraline or placebo, with subsequent flexible dose titration up to 200 mg. The primary outcome is GAD-7 scores at 16 weeks post-randomisation. Secondary outcomes include adverse effects, proportionate change in GAD-7 scores including 50% reduction, social anxiety, obsessive-compulsive symptoms, panic attacks, repetitive behaviours, meltdowns, depressive symptoms, composite depression and anxiety, functioning and disability and quality of life. Carer burden will be assessed in a linked carer sub-study. Outcome data will be collected using online/paper methods via video call, face-to-face or telephone according to participant preference at 16, 24 and 52 weeks post-randomisation, with brief safety checks and data collection at 1–2, 4, 8, 12 and 36 weeks. An economic evaluation to study the cost-effectiveness of sertraline vs placebo and a QuinteT Recruitment Intervention (QRI) to optimise recruitment and informed consent are embedded within the trial. Qualitative interviews at various times during the study will explore experiences of participating and taking the trial medication. Discussion: Results from this study should help autistic adults and their clinicians make evidence-based decisions on the use of sertraline for managing anxiety in this population. Trial registration: ISRCTN, ISRCTN15984604 . Registered on 08 February 2021. EudraCT 2019-004312-66. ANZCTR ACTRN12621000801819. Registered on 07 April 2021.
KW - Adults
KW - Antidepressant
KW - Anxiety
KW - Asperger
KW - Autism
KW - Mental health
KW - Placebo
KW - Randomised controlled trial
KW - Selective Serotonin reuptake inhibitors
KW - Sertraline
UR - http://www.scopus.com/inward/record.url?scp=85182096783&partnerID=8YFLogxK
U2 - 10.1186/s13063-023-07847-3
DO - 10.1186/s13063-023-07847-3
M3 - Article
C2 - 38212784
AN - SCOPUS:85182096783
SN - 1745-6215
VL - 25
JO - Trials
JF - Trials
IS - 1
M1 - 37
ER -