Evidence map›Paper›PMID 40859614›Full record

Trial reportPediatric blood & cancer2025

HABIT Efficacy Trial Intervention Improves Elements of General and Disease-Specific Quality of Life in Youth With Sickle Cell Disease.

Arlene Smaldone, Deepa Manwani, Banu Aygun, Abena Appiah-Kubi, Kim Smith-Whitley, Nancy S Green

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Pediatric blood & cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

6 authors.

Arlene SmaldoneColumbia University School of Nursing, New York, New York, USA.ORCID https://orcid.org/0000-0001-8326-5036
Deepa ManwaniDivision of Hematology, Oncology and Cellular Therapy, Department of Pediatrics, Albert Einstein College of Medicine, New York, New York, USA.ORCID https://orcid.org/0000-0003-1057-1811
Banu AygunNorthwell, New Hyde Park, New York, USA.ORCID https://orcid.org/0000-0001-9934-5161
Abena Appiah-KubiNorthwell, New Hyde Park, New York, USA.
Kim Smith-WhitleyDivision of Hematology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Nancy S GreenDivision of Pediatric Hematology, Oncology and Stem Cell Therapy, Department of Pediatrics, Columbia University Medical Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-9877-1561

Funding

Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment: HABITR01NR017206 · NINR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GREEN, NANCY S., SMALDONE, ARLENE M · 2017 to 2020
$2.9M
NIH HHS 1R01NR017206NINR NIH HHS R01 NR017206
6 · The paper itself

Abstract

backgroundWhether interventions to improve hydroxyurea adherence in youth with sickle cell disease (SCD) also improve health-related quality of life (HRQoL) has not been determined. We prospectively examined changes in generic and disease-specific HRQoL over a 12-month period in youth who participated in "Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT)" randomized controlled multi-site efficacy trial. The HABIT intervention was led by community health workers and augmented by tailored text message reminders.

methodsImprovements in generic and disease-specific HRQoL were secondary HABIT outcomes. Intervention efficacy and sustainability were measured as changes in HRQoL from Months 0 to 9 and from Months 9 to 12 of the trial, respectively. Data were analyzed for within-group and between-group changes.

resultsFifty youth, 24 assigned to intervention and 26 to the control group, mean age of 13.3 ± 1.9 years, participated in the trial. There were no differences between groups at study entry. At Month 0, total generic and disease-specific HRQoL scores were 71.2 ± 15.6 and 62.7 ± 19.0, respectively. At 9 months, compared to controls, the intervention group significantly improved generic HRQoL total score (p = 0.04) and two subscales (emotional, p = 0.03, and social, p = 0.01), and one disease-specific HRQoL subscale (treatment, p = 0.006). HRQoL improvements were not sustained at 12 months.

conclusionsFindings of this study contribute to the evolving understanding of the impact of interventions to improve hydroxyurea adherence on HRQoL in youth with SCD. Further research directed to enhancing intervention sustainability is needed to maintain hydroxyurea adherence and HRQoL improvements to reduce health disparities for youth with SCD.

Indexed as

Anemia, Sickle CellAntisickling AgentsHydroxyureaMedication AdherenceQuality of LifeAdolescentChildFemaleFollow-Up StudiesHumansMalePrognosisProspective StudiesAntisickling AgentsHydroxyureaadherencecommunity health workerhydroxyureaquality of lifesickle cell diseasetext messages

Identifiers

PMID40859614
PMCPMC12832038

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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.