Evidence map›Paper›PMID 42313362›Full record

ArticleJournal of autism and developmental disorders2026

A Qualitative Study of the Treatment Experiences of Autistic Adults Allocated to Sertraline or Placebo for Anxiety in a Blinded Randomised Controlled Trial.

Jade Eloise Norris, Alba X Realpe, Ava Lorenc, Leonora Cotton, Zoe Morgan, Dheeraj Rai, Nicola Mills, STRATA Collaboration Group

Abstract read
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In one paragraph

Article in Journal of autism and developmental disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Jade Eloise Norris *Population Health Sciences, University of Bristol, Bristol, UK. jade.norris@bristol.ac.uk.ORCID http://orcid.org/0000-0002-5096-2692
Alba X Realpe *Population Health Sciences, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0001-9502-3907
Ava LorencPopulation Health Sciences, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-3254-004X
Leonora CottonBristol Trials Centre, University of Bristol, Bristol, UK.ORCID http://orcid.org/0009-0004-2107-0670
Zoe MorganDepartment of Population Health Sciences, University of Leicester, Leicester, UK.ORCID http://orcid.org/0000-0002-6942-1781
Dheeraj RaiPopulation Health Sciences, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-7239-3523
Nicola MillsPopulation Health Sciences, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-2960-2940
STRATA Collaboration Group

Funding

Health Technology Assessment Programme NIHR127337National Health and Medical Research Council GNT1171206
6 · The paper itself

Abstract

purposeThe STRATA randomised-controlled trial (RCT) examined the antidepressant sertraline vs placebo for treating anxiety in autistic adults. Autistic people are often assumed to be reluctant to take part in RCTs due to intolerance of their inherent uncertainty. This study aimed to qualitatively examine autistic people's experiences of RCT participation, specifically regarding their random assignment to an antidepressant (sertraline) or placebo for their mental health, whilst blinded to treatment allocation.

methodsSemi-structured interviews were undertaken with a purposive sample of 62 STRATA participants. The interviews examined why they chose to take part, why they continued in the trial and/or discontinued medication, and their overall experience of participation. Interviews took place either during participation, or at participants' final trial appointment at 52-weeks post randomisation ('exit interviews'). Data were analysed thematically through a collaborative process, with multiple researchers independently coding, discussing, and refining themes.

resultsInterviewees often discussed improved anxiety, attributing changes to believing they were taking sertraline, experiencing the placebo effect, or external factors. Post-analysis unblinding revealed that improved anxiety was discussed equally by participants in both the sertraline and placebo groups. Some participants, including those taking placebo, experienced side effects, which mirrored the types, frequency, and severity seen in the general population. Many were able to manage these and continue, but some discontinued medication as a result.

conclusionAspects of trial design and delivery facilitated continuation with the study medication, including frequent appointments, shared control over medication dose, and meaningfully involving autistic people in trial design. Such non-pharmacological factors may enhance therapeutic benefits, and may improve RCT design and therapeutic alliances with autistic people.

Indexed as

AntidepressantAutismBlindingPlaceboRandomised controlled trialSertraline

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.