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Preregistration Template — OSF Standard 21-Item Preregistration Template
Purpose
A fill-in template based on the OSF Standard Pre-Data Collection Registration format. Researchers complete this template before data collection and upload it to a preregistration platform (e.g., OSF Registries).
Instructions
- Complete this template before data collection
- Items marked
[Required]are mandatory;[Optional]are recommended but not required - If an item is not applicable, write "Not applicable" and briefly explain why
- After completion, go to OSF Registries to create a preregistration
- Once submitted, preregistrations cannot be modified (an embargo period can be set)
A. Study Information
1. Title [Required]
Study Title
[Enter descriptive study title]
2. Authors [Required]
Research Team
| Name | Institution | Role | ORCID |
|---|---|---|---|
| [Name] | [Institution] | [PI / Co-PI / RA] | [ORCID] |
| [Name] | [Institution] | [Role] | [ORCID] |
3. Research Questions [Required]
Main Research Questions
RQ1: [Enter main research question]
RQ2: [Enter secondary research question, if any]
4. Hypotheses [Required]
Pre-specified Hypotheses Please state directional predictions clearly
H1: [Enter hypothesis 1, including expected direction]
Example: Students receiving treatment X will score significantly higher
on test Y than the control group
H2: [Enter hypothesis 2, if any]
H3: [Enter hypothesis 3, if any]
B. Design Plan
5. Study Type [Required]
Study Design
- Experiment
- Between-subjects
- Within-subjects
- Mixed design
- Factorial design: ___ x ___
- Observational study
- Cross-sectional
- Longitudinal / Cohort
- Case-control
- Survey
- Other: [Describe]
[Describe study design in detail]
6. Randomization [Optional]
Randomization Procedure
Randomization method: [Simple random / Stratified random / Cluster random / Block random / Not applicable]
Randomization unit: [Individual / Class / School / Not applicable]
Randomization tool: [Random number table / Computer program / Lottery / Not applicable]
Allocation ratio: [1:1 / 2:1 / Other]
7. Blinding [Optional]
Blinding / Masking
Blinding level: [No blinding / Single-blind / Double-blind / Triple-blind]
Blinded parties: [Participants / Researchers / Assessors / Not applicable]
Blinding maintenance: [Describe how blinding is maintained]
Unblinding timing: [Describe when unblinding occurs]
8. Study Design / Conditions [Required]
Specific description of each group/condition
Experimental group/Condition 1: [Describe intervention content, duration, frequency in detail]
Experimental group/Condition 2: [If any]
Control group: [Describe control condition in detail]
C. Sampling Plan
9. Existing Data [Required]
Existing Data Declaration
- No data have been collected yet (Registration prior to creation of data)
- Data exist but have not been examined (Registration prior to any human observation of the data)
- Some data have been examined (Registration prior to accessing the data)
- Data have been used for preliminary analysis (Registration following analysis of the data)
[Describe data status and your level of familiarity with the data]
10. Data Collection Procedures [Required]
Data Collection Procedures
Collection method: [Online survey / Paper survey / Interview / Experiment / Archival data / Other]
Collection instruments: [Questionnaire name / Scale name / Experimental software]
Collection location: [Online / Classroom / Laboratory / Other]
Collection timeline: [Start and end dates]
Data collectors: [Who is responsible for collection]
11. Sample Size [Required]
Planned sample size
Target sample size: [N = ]
Sample size per group: [Experimental group n = , Control group n = ]
12. Sample Size Rationale [Required]
Basis for sample size determination
Method: [Power analysis / Prior research conventions / Feasibility constraints / Other]
Power analysis parameters (if applicable):
- Effect size: [d = / f = / r = ]
- Effect size source: [Prior study / Meta-analysis / Pilot study]
- Significance level (alpha): [.05 / .01]
- Statistical power: [.80 / .90]
- Test type: [t-test / ANOVA / Regression / Other]
- Calculation tool: [G*Power / R / Other]
- Calculation result: Minimum required N = [ ]
Oversampling rate: [Accounting for ___% attrition, actual target N = ]
13. Stopping Rule [Required]
When to stop data collection
Stopping rule:
- [ ] Stop when target sample size is reached
- [ ] Stop at specified date (Deadline: [Date])
- [ ] Stop when target power is reached (sequential analysis)
- [ ] Other: [Describe]
D. Variables
14. Manipulated Variables [Required for experiments]
Independent Variables
Independent variable 1: [Name]
Operational definition: [How it is manipulated]
Levels: [Level 1 / Level 2 / ...]
Independent variable 2: [If any]
15. Measured Variables [Required]
Dependent Variables
Primary dependent variable: [Name]
Operational definition: [How it is measured]
Measurement instrument: [Scale name / Test name]
Reliability and validity: [Cite reliability/validity literature]
Secondary dependent variable: [If any]
Covariates/Control variables: [If any]
16. Indices [Required]
Specific scoring method for each variable
Variable 1 scoring:
- Items: [Which items]
- Scoring method: [Sum / Mean / Factor score / Other]
- Reverse-scored items: [Which items need reverse scoring]
- Missing data handling: [How to handle missing values]
Variable 2 scoring: [Same format as above]
E. Analysis Plan
17. Statistical Models [Required]
Primary statistical analysis methods
Analysis for Hypothesis 1:
- Statistical method: [Independent t-test / ANOVA / Regression / HLM / SEM / Other]
- Detailed description: [Model specification, e.g., DV ~ IV + covariate + (1|cluster)]
Analysis for Hypothesis 2: [Same format as above]
18. Transformations [Optional]
Data transformation plan
Planned transformations:
- [ ] No transformations
- [ ] Log transformation: Applied to [which variables], trigger condition [skewness > ]
- [ ] Standardization (Z-score)
- [ ] Other: [Describe]
19. Inference Criteria [Required]
Statistical inference criteria
Significance level: alpha = [.05 / .01 / .005]
Multiple comparison correction: [Bonferroni / Holm / FDR / Not applicable]
Effect size reporting: [Cohen's d / eta-squared / R² / Other]
Confidence interval: [95% CI / 99% CI]
One-tailed/Two-tailed test: [Two-tailed / One-tailed, with justification]
20. Data Exclusion [Required]
Data exclusion criteria
Exclusion criteria:
- [ ] Failed attention check (Specific criteria: [ ])
- [ ] Response time too short/long (Criteria: < [ ] minutes or > [ ] minutes)
- [ ] Outliers (Definition: [> 3 SD / IQR method / Other])
- [ ] Incomplete rate > [ ]%
- [ ] Other: [Describe]
Post-exclusion procedures:
- Report pre- and post-exclusion sample sizes
- Compare characteristics of excluded vs. retained samples
21. Exploratory Analyses [Optional]
Planned exploratory analyses
Exploratory analyses (not primary hypotheses, but planned):
1. [Analysis description]
2. [Analysis description]
These analyses will be explicitly labeled as "exploratory" in the paper.
F. Other
Ethics Review [Optional]
IRB review status: [Approved / Under review / Exempt / Not applicable]
IRB number: [ ]
Reviewing institution: [ ]
Data Availability [Optional]
Will data be made public: [Yes / No / Partially]
Data repository: [OSF / Dataverse / Other]
Timing: [After publication / After study completion / Other]
Supplementary Materials [Optional]
- [ ] Full questionnaire/scale
- [ ] Stimulus materials
- [ ] Analysis code
- [ ] Power analysis report
- [ ] Pilot study results
Pre-Submission Checklist
- All [Required] items have been completed
- Hypotheses are clearly stated and testable
- Analysis methods correspond to hypotheses
- Exclusion criteria were established before data collection
- Confirmatory and exploratory analyses have been distinguished
- IRB review status has been confirmed
- Preregistration platform has been selected (OSF Registries recommended)
After completion, go to OSF Registries to submit the preregistration.