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Deidentified Individual Participant Data Set (IPD)
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Yes - There is a plan to make this available
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Study Protocol
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Yes - There is a plan to make this available
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Statistical Analysis Plan
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Yes - There is a plan to make this available
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Informed Consent Form
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Yes - There is a plan to make this available
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Clinical Study Report
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Not applicable
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Analytic Code
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Yes - There is a plan to make this available
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Data Dictionary
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Yes - There is a plan to make this available
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Title and more details about the data/document
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De-identified Participant Data: An anonymized dataset including participant codes, demographic information, and pretest and posttest scores for depression, dysfunctional beliefs, and self-esteem.
Study Protocol:The study protocol including the research objectives, methodology, inclusion and exclusion criteria, description of the Mindfulness-Based Cognitive Therapy (MBCT) intervention, and outcome measures.
Statistical Analysis Plan:A statistical analysis plan describing the methods used to analyze the data and compare the experimental and control groups at the pretest and posttest stages.
Informed Consent Form:The participant information sheet and informed consent form used in the study (Persian version).
Analytical Codes: SPSS syntax files used for data entry, cleaning, management, and statistical analysis.
Data Dictionary: A data dictionary defining the variables included in the anonymized dataset, including variable names, definitions, data types, and coding schemes.
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When the data will become available and for how long
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The data and documents will become publicly available upon acceptance for publication of the primary results manuscript. They will be stored with no end date for access.
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To whom data/document is available
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Available to researchers, students, and meta-analysts in the scientific community worldwide.
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Under which criteria data/document could be used
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Data and documents may be used for non-commercial, scientific purposes such as validation, meta-analysis, methodological research, or educational purposes. Any proposed use must be approved by an independent scientific review committee and must comply with ethical standards.
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From where data/document is obtainable
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The documents (Protocol, SAP, Consent Form) will be attached to the trial registration on the Iranian Registry of Clinical Trials (IRCT). The final, shareable versions of all items will be deposited in a public, open-access repository such as Mendeley Data, Figshare, or Zenodo. A direct link (DOI) will be provided in the published manuscript and updated in this registry entry.
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What processes are involved for a request to access data/document
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For the deidentified IPD: A managed access process is required. Requestors must submit a brief proposal outlining their intended use, analysis plan, and ethical approval to the Corresponding Author (Dr. Mehdi Amiri) via email. Requests will be reviewed by the study's principal investigator within 4 weeks. Approved requestors will be granted access via the repository with a unique token or will receive the data directly.
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Comments
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