纳入和排除标准数据集

数据集获取（Figshare）

• 源站标题：Inclusion and exclusion criteria.
• DOI：10.1371/journal.pone.0329883.t001
• 发布日期：2025-10-24
• 文件数：1 个
• 文件总体积：5.63 KB
• 源站页面：https://plos.figshare.com/articles/dataset/Inclusion_and_exclusion_criteria_/30440335

命令行下载

curl -L -o "Table 1.xls" "https://ndownloader.figshare.com/files/59029498"

文件清单

• Table 1.xls（5.63 KB）

文件总体积 5.63 KB（源站 API 实测）。

数据加载示例（图像类）

from PIL import Image
import glob, os

files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)

# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path)  # 要求 子目录=类别

目录组织与标注格式以源站说明和下载后实际文件为准。

数据说明

The number of patients who suffer from pelvic floor disorders increases with age and can have a significant impact on quality of life. The first-line treatment for these different disorders includes pelvic floor rehabilitation. However, there are high rates of non-compliance with completing the recommended duration of treatment due to delays in appointments and time constraints. Thus, the primary goal of this study is to evaluate the feasibility and acceptability of an online eight-week video-based pelvic floor muscle therapy program. A secondary goal is determining whether the treatment can improve quality of life and symptoms. This study is a registry-based pilot single-arm prospective trial (NCT06689891: Video-Based Pelvic Floor Muscle Therapy). A single-arm design was utilized because our primary aim was to assess feasibility rather than comparative efficacy. Methodical guidance recommends a single-arm approach when outcomes focus on process measures instead of hypothesis testing. This design allows us to evaluate whether the intervention can be delivered as intended, establish feasibility before a larger trial, and maintain flexibility for modification without compromising a control group. Eligible participants will be offered the online program as an alternative to in-person pelvic floor rehabilitation. Primary timepoints include a pre-intervention in-person visit with a licensed pelvic floor therapist and the 8-week video-based pelvic floor muscle therapy program. There will be a midpoint evaluation followed by a post-intervention visit with the same pelvic floor therapist, where participants will be graded on their ability to complete the various exercises to assess efficacy. A survey assessing the online-based program’s usability will be conducted post-intervention. Patient-reported outcome measures, including quality of life and symptom changes, will be collected pre-, mid-, and post-intervention. As this is a pilot trial, the goal is to establish the acceptability and feasibility of a video-based pelvic floor muscle therapy program as an alternative to in-person treatment.

许可

CC BY 4.0

引用

学术使用请引用 DOI 10.1371/journal.pone.0329883.t001（source: https://plos.figshare.com/articles/dataset/Inclusion_and_exclusion_criteria_/30440335）。