ReadMe file for the meta-analysis of attentional bias to somaotosensory stimuli in chronic pain patients There are 13 csv files which include the data from the meta-analysis and risk of bias analysis. File descriptions: 1 somatosensory modality ab chronic pain vs healthy.csv = data for attentional bias to somatosensory modality stimuli over other modalities 1a painful stimuli.csv = data for attentional bias to painful somatosensory modality stimuli over other modalities 1b non-painful stimuli.csv = data for attentional bias to non-painful somatosensory modality stimuli over other modalities 1c attentional interference.csv = data for attentional bias to somatosensory modality stimuli over other modalities from the primary task paradigm 1d distraction efficacy.csv = data for attentional bias to somatosensory modality stimuli over other modalities from the common task paradigm 2 spatial ab affected vs unaffected.csv = data for spatial attentional bias to somatosensory stimuli on the pain-affected side as compared to the pain-free side 3 spatial ab chronic pain vs healthy.csv = data for spatial attentional bias to somatosensory stimuli compared between chronic pain and healthy people 4 visual ab affected vs unaffected.csv = data for spatial attentional bias to visual stimuli compared between chronic pain and healthy people between-group modality.csv = data from all between-group modality studies for publication bias analysis between-group spatial.csv = data from all between-group spatial studies for publication bias analysis within-group studies.csv = data from all within-group spatial studies for publication bias analysis risk of bias date ordered.csv = risk of bias ratings in chronological order rob_ratings.csv = agreement of risk of bias ratings between the two independent raters Relationships between files: Data is in the input folder, R scripts are in the R folder and plots generated are sent to the graphics folder. Definitions of variable names meta-analysis data: label = short name of the study the data refers to m1i = chronic pain mean for between-group data/pain affected side mean for within-group data sd1i = chronic pain standard deviation for between-group data/pain affected side standard deviation for within-group data m2i = healthy mean for between-group data/pain unaffected side mean for within-group data sd2i = healthy standard deviation for between-group data/pain unaffected side standard deviation for within-group data n1i = sample size of chronic pain group for between-group data/overall sample size for within-group data n2i = sample size of healthy group for between-group data/overall sample size for within-group data stimuli_location = bodily location to which stimuli were presented stimuli_type = type of stimulus stimuli_pain = yes/no variable indicating whether the stimuli were painful paradigm = the task/paradigm used to assess attentional bias age_mean = mean age of the participants percent_female = percentage of the participants who were female condition = chronic pain condition of the participants pain_duration = mean pain duration of the participants in months pain_intensity = mean rating of pain intensity scaled from 0-10 risk of bias data: author = short name of the study the data refers to replicable_sampling_method = could the sampling method be replicated (low, high, or unclear risk of bias) recognised_diagnosis_criteria = were recognised diagnosis criteria used for participant recruitment (low, high, or unclear risk of bias) matched_controls = were healthy controls matched with the chronic pain patients in age and gender (low, high, or unclear risk of bias) researcher_blinded = was the researcher who analysed the data unaware of whether each participant was in the healthy or chronic pain group (low, high, or unclear risk of bias) replicable_method = could the method be replicated (low, high, or unclear risk of bias) paradigm_validated = had the task been previously validated for use with this population (low, high, or unclear risk of bias) power_calc = was an a priori power calculation conducted to determine sample size (low, high, or unclear risk of bias) missing_data_dealt_with = was the strategy for missing data determined a priori/there was no missing data (low, high, or unclear risk of bias) all_outcomes_reported = were all outcomes included in the methods section reported in the results (low, high, or unclear risk of bias) PB = risk of bias ratings from one researcher DS = risk of bias ratings from another independent researcher Final = the rating agreed upon by both researchers Definitions of row names: Sinforani et al. 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