Evidence map›Paper›PMID 42565481›Full record

Trial reportPsycho-oncology2026

Adaptive, Stepped-Care for Cancer-Related PTSD Symptoms in HCT Survivors: Results From a SMART Trial.

Sophia K Smith, Eric Kuhn, Tamara J Somers, Eric Laber, Cole Manschot, Anthony D Sung, Sarah A Kelleher, Catherine Majestic, Karen L Syrjala, Deborah Mayer and 6 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Psycho-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04058795 (Using a SMART Design to Optimize PTSD Symptom Management Strategies Among Cancer Survivors), which is not on this map. Not yet cited in PubMed.

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

NCT04058795 nacompletednot on this map

Using a SMART Design to Optimize PTSD Symptom Management Strategies Among Cancer Survivors

TypeinterventionalSponsorDuke UniversityRan2021 to 2025Enrolled524ConditionsPosttraumatic Stress Disorder, CancerArmsCancer Distress Coach (CaDC) App, CaDC + mCoaching, mCBT
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Sophia K SmithSchool of Nursing, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-7809-0339
Eric KuhnDissemination and Training Division, National Center for PTSD, Palo Alto, California, USA.
Tamara J SomersDuke Cancer Institute, Duke University Medical Center, Durham, North Carolina, USA.
Eric LaberDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.ORCID 0000-0003-2640-7696
Cole ManschotBiostatistics and Research Decision Sciences (BARDS), Merck & Co., Inc., Rahway, New Jersey, USA.ORCID 0000-0002-5054-2663
Anthony D SungDepartment of Medicine, Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, Kansas, USA.
Sarah A KelleherDuke Cancer Institute, Duke University Medical Center, Durham, North Carolina, USA.
Catherine MajesticDuke Cancer Institute, Duke University Medical Center, Durham, North Carolina, USA.ORCID 0000-0001-5661-1853
Karen L SyrjalaClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Deborah MayerSchool of Nursing, University of North Carolina, Chapel Hill, North Carolina, USA.
Sergio GiraltMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Andrea PiresSchool of Nursing, Duke University, Durham, North Carolina, USA.
Rebecca R GebertDepartment of Psychological and Brain Sciences, Boston University, Boston, Massachusetts, USA.ORCID 0000-0002-7069-5405
Jason E OwenDissemination and Training Division, National Center for PTSD, Palo Alto, California, USA.
Jean C YiClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.ORCID 0000-0003-4589-7272
Allison J ApplebaumBrookdale Department of Geriatrics and Palliative Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.ORCID 0000-0002-2140-5635

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Using a SMART Design to Optimize PTSD Symptom Management Strategies Among Cancer SurvivorsR01CA244172 · NCI · DUKE UNIVERSITY · PI SMITH, SOPHIA K. · 2020 to 2024
$3.2M
Next-generation SMARTs for Discovery and Evaluation of Sequential Cancer Therapeutic StrategiesR01CA280970 · NCI · DUKE UNIVERSITY · PI Eric Benjamin Laber · 2024 to 2026
$1.1M
NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA244172NCI NIH HHS R01-CA244172NCI NIH HHS R01 CA280970
6 · The paper itself

Abstract

objectiveCancer-related posttraumatic stress disorder (PTSD) is prevalent among hematopoietic cell transplantation (HCT) survivors, yet access to evidence-based care is limited. This study evaluated adaptive, stepped-care treatment sequences for PTSD symptoms using a Sequential Multiple Assignment Randomized Trial (SMART), comparing digital and therapist-delivered interventions.

methodsHCT survivors (N = 477), 1-5 years post-transplant, with probable or subthreshold PTSD, were randomized to the Cancer Distress Coach (CaDC) app or Usual Care. At Week 4, non-responders (i.e., < 5-point PCL-5 reduction) were re-randomized to CaDC + Coaching or therapist-delivered cognitive behavioral therapy for PTSD (CBT-PTSD). PTSD symptoms (primary outcome), depression, and anxiety were assessed at baseline, Week 4, Month 3 (primary endpoint), and Month 6.

resultsBoth initial treatment groups demonstrated symptom reductions at Week 4 with no significant between-group differences; approximately 60% met early response criteria. By Month 3, outcomes reflected treatment escalation rather than direct comparison of initial interventions. Regimen-level analyses demonstrated differences across adaptive sequences for PTSD at Months 3 and 6, and for depression and anxiety at Month 3 (global p-values ≤ 0.018). Regimens escalating to CBT-PTSD were associated with greater and more sustained reductions than those escalating to CaDC + Coaching. The sequence initiating with CaDC and escalating to CBT-PTSD produced the largest effects.

conclusionsAlthough a self-guided digital intervention did not outperform Usual Care initially, adaptive stepped-care strategies that triage early responders and escalate non-responders to therapist-delivered CBT-PTSD were associated with the greatest reductions in symptoms. Digital tools may function as entry points within stepped-care models to allocate higher-intensity psychotherapy. TRIALS REGISTRATION: ClinicalTrials.gov, NCT04058795, registered 8/16/2019.

Indexed as

Cancer SurvivorsCognitive Behavioral TherapyHematopoietic Stem Cell TransplantationNeoplasmsStress Disorders, Post-TraumaticAdultAgedAnxietyDepressionFemaleHumansMaleMiddle AgedMobile ApplicationsTreatment Outcomeadaptive interventioncancer distress coachcancer‐related PTSDdigital CBThematopoietic cell transplantationmobile healthPCL‐5SMARTstepped‐caresurvivorship

Identifiers

PMID42565481
PMCPMC13449622

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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 OpenQuestion graph.