Lauren E Powell, Erica M Bien, Madison Kolbow, Ruth J Barta
{"title":"照顾者对唇裂和/或腭裂儿童患者教育材料的偏好。","authors":"Lauren E Powell, Erica M Bien, Madison Kolbow, Ruth J Barta","doi":"10.1177/10556656251332213","DOIUrl":null,"url":null,"abstract":"<p><p>ObjectiveTo determine caregiver preferences for education modalities.Design/SettingA cross-sectional study of caregivers of patients with cleft lip and/or palate (CL/P) seen at this American Cleft Palate-Craniofacial Association-approved center in the Midwest between January 2017 and September 2022 was conducted.Patients/ParticipantsThe population included parents of patients undergoing primary or secondary revision surgeries after a diagnosis of CL/P.Main Outcome MeasuresA phone interview gathered demographics, education preferences, familial research, and resources.ResultsOf the 81 families of CL/P patients, 42 families consented for interviews. Patients first presented to the clinic at an average age of 2.3 years of age (range 0-17) and had a mean age of 10.1 years (range 1-23) at the time of parental interview. The majority of interviewees identified as the patient's mother (90.5%), Caucasian (78.6%), and had completed a college education (81%). The majority (85.7%) of caregivers reported completing research prior to the first appointment. Most participants preferred electronic resources (35.7%), support groups (29%), books or written material (29%), with fewer preferring videos (12%), social media (7%), or podcasts (2%).ConclusionThe majority of families preferred having multiple resources available to learn about CL/P; however, the most common preferences were additional books, pamphlets, and online materials such as websites, videos, and audiobooks. With the multitude of options available for patient education materials, designing and providing high-quality materials that will be used by families and meet the health literacy of this diverse patient population is crucial.</p>","PeriodicalId":49220,"journal":{"name":"Cleft Palate-Craniofacial Journal","volume":" ","pages":"10556656251332213"},"PeriodicalIF":1.1000,"publicationDate":"2025-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Caregiver Preferences Toward Patient Education Materials for Children With Cleft Lip and/or Palate.\",\"authors\":\"Lauren E Powell, Erica M Bien, Madison Kolbow, Ruth J Barta\",\"doi\":\"10.1177/10556656251332213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>ObjectiveTo determine caregiver preferences for education modalities.Design/SettingA cross-sectional study of caregivers of patients with cleft lip and/or palate (CL/P) seen at this American Cleft Palate-Craniofacial Association-approved center in the Midwest between January 2017 and September 2022 was conducted.Patients/ParticipantsThe population included parents of patients undergoing primary or secondary revision surgeries after a diagnosis of CL/P.Main Outcome MeasuresA phone interview gathered demographics, education preferences, familial research, and resources.ResultsOf the 81 families of CL/P patients, 42 families consented for interviews. Patients first presented to the clinic at an average age of 2.3 years of age (range 0-17) and had a mean age of 10.1 years (range 1-23) at the time of parental interview. The majority of interviewees identified as the patient's mother (90.5%), Caucasian (78.6%), and had completed a college education (81%). The majority (85.7%) of caregivers reported completing research prior to the first appointment. Most participants preferred electronic resources (35.7%), support groups (29%), books or written material (29%), with fewer preferring videos (12%), social media (7%), or podcasts (2%).ConclusionThe majority of families preferred having multiple resources available to learn about CL/P; however, the most common preferences were additional books, pamphlets, and online materials such as websites, videos, and audiobooks. With the multitude of options available for patient education materials, designing and providing high-quality materials that will be used by families and meet the health literacy of this diverse patient population is crucial.</p>\",\"PeriodicalId\":49220,\"journal\":{\"name\":\"Cleft Palate-Craniofacial Journal\",\"volume\":\" \",\"pages\":\"10556656251332213\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2025-04-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cleft Palate-Craniofacial Journal\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/10556656251332213\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Dentistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cleft Palate-Craniofacial Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/10556656251332213","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Dentistry","Score":null,"Total":0}
Caregiver Preferences Toward Patient Education Materials for Children With Cleft Lip and/or Palate.
ObjectiveTo determine caregiver preferences for education modalities.Design/SettingA cross-sectional study of caregivers of patients with cleft lip and/or palate (CL/P) seen at this American Cleft Palate-Craniofacial Association-approved center in the Midwest between January 2017 and September 2022 was conducted.Patients/ParticipantsThe population included parents of patients undergoing primary or secondary revision surgeries after a diagnosis of CL/P.Main Outcome MeasuresA phone interview gathered demographics, education preferences, familial research, and resources.ResultsOf the 81 families of CL/P patients, 42 families consented for interviews. Patients first presented to the clinic at an average age of 2.3 years of age (range 0-17) and had a mean age of 10.1 years (range 1-23) at the time of parental interview. The majority of interviewees identified as the patient's mother (90.5%), Caucasian (78.6%), and had completed a college education (81%). The majority (85.7%) of caregivers reported completing research prior to the first appointment. Most participants preferred electronic resources (35.7%), support groups (29%), books or written material (29%), with fewer preferring videos (12%), social media (7%), or podcasts (2%).ConclusionThe majority of families preferred having multiple resources available to learn about CL/P; however, the most common preferences were additional books, pamphlets, and online materials such as websites, videos, and audiobooks. With the multitude of options available for patient education materials, designing and providing high-quality materials that will be used by families and meet the health literacy of this diverse patient population is crucial.
期刊介绍:
The Cleft Palate-Craniofacial Journal (CPCJ) is the premiere peer-reviewed, interdisciplinary, international journal dedicated to current research on etiology, prevention, diagnosis, and treatment in all areas pertaining to craniofacial anomalies. CPCJ reports on basic science and clinical research aimed at better elucidating the pathogenesis, pathology, and optimal methods of treatment of cleft and craniofacial anomalies. The journal strives to foster communication and cooperation among professionals from all specialties.