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1,364 results for “RCT”
PsPM-DoxMem1: SCR, ECG and respiration measurements in an RCT using doxycycline/placebo during delay fear conditioning and retention.
<p>This dataset includes skin conductance response (SCR), electrocardiogram (ECG), respiration and electromyogramm (EMG, only relevant for retention phase) measurements. Also included are CS and US information, keypress responses and keypress response times for 78 healthy participants (40 males and 38 females aged 23.3+/-3.6 years) under either doxycycline or placebo during a classical (Pavlovian) discriminant delay fear conditioning task. CS were a red and a blue screen. US consisted of 0.5 s square electric pulses with participant-specific duration and 500 Hz frequency. SOA between the CS onset and US was 3.5 s. CS and US co-terminated. Before the fear conditioning task, participants completed an N-back task and several questionnaires. During the retention/extinction phase one week after learning and without drug, an auditory startle probe (ST) and no US was delivered 3.5 s after CS onset via headphones (100 dB, 50 ms duration with 2ms on- and offset ramp). In an immediately following re-learning phase, the ST was omitted and the CS reinforced with the same schedule as during acquisition. The ITI was randomly determined on each trial to be 7, 9, or 11 s.</p>
RCT NOVICE Surgeon training Lübeck Toolbox
<p>Surgeon residents were rated by GOALS score at their first operations by masked raters. Some had trained with the Lübeck Toolbox until sufficiently proficient in a waiting group design. </p> <p>The <em><strong>study protocol</strong></em> was published here: <a title="Persistent link using digital object identifier" href="https://doi.org/10.1016/j.isjp.2020.02.004" target="_blank" rel="noreferrer noopener">https://doi.org/10.1016/j.isjp.2020.02.004</a></p> <p>The article with the <em><strong>results</strong></em> is published here: <a href="http://dx.doi.org/10.1097/JS9.0000000000002304">http://dx.doi.org/10.1097/JS9.0000000000002304</a> </p>
Data of 14 participants in the RCT titled Acute effects of virtual reality exercise bike games on psychophysiological outcomes in college North-African adolescents with cerebral palsy: A randomized clinical trial
<p>It is an Excel file including the numerical data of the 14 participants included in the study titled: <a name="_Hlk151119211"></a><span>Acute effects of virtual reality exercise bike games on psychophysiological outcomes in college North-African adolescents with cerebral palsy: A randomized clinical trial</span></p>
The impact of pharmaceutical form and simulated side effects in an open-label-placebo RCT for improving psychological distress in highly stressed students (Open Data and Open Materials)
<p> Open-label placebo (OLP) may be utilized to reduce psychological distress. Yet, potential contextual effects have not been explored. We investigated the impact of pharmaceutical form and the simulation of side effects in a parallel group RCT (DRKS00030987). A sample of 177 highly stressed university students at risk of depression were randomly assigned by computer generated tables to a one-week intervention with active or passive OLP nasal spray or passive OLP capsule or a no-treatment control group. After the intervention, groups differed significantly in depressive symptoms but not regarding other outcomes of psychological distress (stress, anxiety, sleep quality, somatization), well-being or treatment expectation. OLP groups benefitted significantly more compared to the no-treatment control group (<em>d</em>=.40), OLP nasal spray groups significantly more than the OLP capsule group (<em>d</em>=.40) and the active OLP group significantly more than the passive OLP groups (<em>d</em>=.42). Interestingly, before intervention, most participants, regardless of group assignment, believed that the OLP capsule would be most beneficial. The effectiveness of OLP treatments seems to be highly influenced by the symptom focus conveyed by the OLP rationale. Moreover, pharmaceutical form and simulation of side effects may modulate efficacy, while explicit treatment expectation seems to play a minor role.</p>
Ablauf einer RCT-Studie
<p>Ablauf einer RCT-Studie für zwei Arme bzw. Gruppen (Interventions- und Kontrollgruppe), unter Berücksichtigung einer zufälligen Zuweisung in die Gruppen (Randomisierung). Die RCT-Studie ist der Goldstandard für die Darstellung / den Beweis von Wirksamkeit bzw. Kausalität.</p>
Procedure of a RCT study
<p>Procedure of a RCT study for two arms or groups (intervention and control group), taking into account random assignment into the groups (randomization). The RCT study is the gold standard for the presentation / proof of efficacy or causality.</p>
RCT of CBD for Anxiety in Advanced Breast Cancer
ClinicalTrials.gov study NCT04482244. IPD Sharing: YES. Countries: 1. Publications: 1.
The BE WITH Project: A Partially Nested Randomized Control Trial (PN-RCT)
ClinicalTrials.gov study NCT07204444. IPD Sharing: NO. Countries: 1. Publications: 26.
RCT for Innovating Stress-related eHealth
ClinicalTrials.gov study NCT05305235. IPD Sharing: YES. Countries: 1. Publications: 2.
Village-level data for the Honduras 176 RCT
Open the record for dataset details and reuse information.
TIMCI India RCT dataset
<p>This dataset contains data from the TIMCI (Tools for Integrated Management of Childhood Illness) cluster Randomized Controlled Trial (RCT) in India (NCT04910750), which was conducted by King George's Medical University (KGMU) in collaboration with the Swiss Tropical & Public Health Institute (Swiss TPH). Data were collected using ODK between <span>June 20, 2022 to April 21, 2023 </span>(10 months) in 106 facilities.</p> <p>To request access to this dataset:</p> <ol> <li>Contact the TIMCI consortium directly</li> <li>Clearly state your intended purpose for data analysis</li> </ol> <p>When using the data, please ensure proper attribution.</p>
DIHnamic proyect RCT Follow up questionnaire
<p>The DIHnamic Project has carried out under the framework of a European initiative that aims to provide innovation support to European agencies as key intermediary agents with small and medium-sized enterprises (SMEs). Innovation in the said agencies is becoming increasingly relevant, with the arrival of new business models and emerging technologies, having to adapt and innovate the way in which support to SMEs is delivered.</p> <p>In addition, this programme has aimed to analyse with an evidence-based approach, using methodologies that provide a rigorous impact measurement, such as RCTs.</p> <p>The impact of this project has been analysed through a Randomised Control Trial, which is a requisite for the evaluation of all projects funded under this call. </p> <p>The baseline information started to be collected since the publication of the results of the call for proposals, where each company was assigned to one of the two services. Filling in the baseline questionnaire was a requisite to accept the support. </p> <p>The baseline and follow-up questionnaires were completed through an online platform set up for this purpose. A protocol for its correct application was also provided in which it was specified that, regardless who completed the online questionnaire, it should have been validated and consolidated by the company's management team, as a key agent in decision-making on digitalisation, and a common agent for all companies.</p>
DIHnamic proyect RCT Baseline questionnaire
<p>The DIHnamic Project has carried out under the framework of a European initiative that aims to provide innovation support to European agencies as key intermediary agents with small and medium-sized enterprises (SMEs). Innovation in the said agencies is becoming increasingly relevant, with the arrival of new business models and emerging technologies, having to adapt and innovate the way in which support to SMEs is delivered.</p> <p>In addition, this programme has aimed to analyse with an evidence-based approach, using methodologies that provide a rigorous impact measurement, such as RCTs.</p> <p>The impact of this project has been analysed through a Randomised Control Trial, which is a requisite for the evaluation of all projects funded under this call. </p> <p>The baseline information started to be collected since the publication of the results of the call for proposals, where each company was assigned to one of the two services. Filling in the baseline questionnaire was a requisite to accept the support. </p> <p>The baseline and follow-up questionnaires were completed through an online platform set up for this purpose. A protocol for its correct application was also provided in which it was specified that, regardless who completed the online questionnaire, it should have been validated and consolidated by the company's management team, as a key agent in decision-making on digitalisation, and a common agent for all companies.</p>
TIMCI Tanzania RCT dataset
<p>This dataset contains data from the TIMCI (Tools for Integrated Management of Childhood Illness) cluster Randomized Controlled Trial (RCT) in Tanzania (NCT04910750), which was conducted by the Ifakara Health Institute (IHI) in collaboration with the Swiss Tropical & Public Health Institute (Swiss TPH). Data were collected with ODK between March 28, 2022 and March 31, 2023 (12 months) in 66 facilities.</p> <p>To request access to this dataset:</p> <ol> <li>Contact the TIMCI consortium directly</li> <li>Clearly state your intended purpose for data analysis</li> </ol> <p>When using the data, please ensure proper attribution.</p>
Raw deidentified data ByarsWinston R01 RCT
<p>Raw deidentified data file in SPSS for R01 RCT data published in <em>Science Advances</em></p>
DYNAMIC TZ Cluster RCT Dataset
<p>De-identified dataset from the DYNAMIC Tanzania cluster-randomized controlled trial evaluating the impact of the ePOCT+ package on antibiotic prescription (superiority analysis) and clinical failure (non-inferiority analysis) compared to usual care. Study conducted in the Mbeya and Morogoro regions of Tanzania between December 2021 to October 2022.</p>
An RCT Comparing Xenograft and Allograft for Ridge Preservation
ClinicalTrials.gov study NCT02330523. IPD Sharing: Not stated. Countries: 1. Publications: 1.
A Comparative Effectiveness RCT of Optimized Cessation Treatments
ClinicalTrials.gov study NCT02301403. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Pragmatic RCT of High-dose Oral Montelukast for Moderate and Severe Pediatric Acute Asthma Exacerbations
ClinicalTrials.gov study NCT03277170. IPD Sharing: YES. Countries: 1. Publications: 1.
VR for Pain & Sleep in Burn Patients: A RCT
ClinicalTrials.gov study NCT07306442. IPD Sharing: YES. Countries: 1. Publications: 2.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.