Content validity–establishing and reporting the evidence in newly developed patient‐reported outcomes (PRO) instruments for medical product evaluation: ISPOR PRO good research practices task force report: part 1 – eliciting concepts for a new PRO instrument

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Items 401–500 of 1,000

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2. Qualitative Interviews to Support Development and Cognitive Debriefing of the Adelphi Adherence Questionnaire (ADAQ©): A Patient-Reported Measure of Medication Adherence Developed for Use in a Range of Diseases, Treatment Modalities, and Countries
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4. “Keep it simple”: Perspectives of patients with low back pain on how to qualify a patient‐centred consultation using patient‐reported outcomes
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5. Concepts Important to Patients With Facial Differences: A Qualitative Study Informing a New Module of the FACE-Q for Children and Young Adults
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6. Construction of a conceptual framework for assessment of health-related quality of life in calves with respiratory disease.
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7. The Intestinal Gas Questionnaire: development of a new instrument for measuring gas‐related symptoms and their impact on daily life
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8. Initial Development and Content Validation of a Health-Related Symptom Index for Persons either Treated or Monitored for Anal High-Grade Squamous Intraepithelial Lesions
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11. Patient-reported outcomes in hidradenitis suppurativa
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12. Danish and Dutch linguistic validation and cultural adaptation of the WOUND-Q, a PROM for chronic wounds
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13. Three wound-dressing strategies to reduce surgical site infection after abdominal surgery: the Bluebelle feasibility study and pilot RCT
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14. Systematic Assessment of Adult Patients’ Satisfaction with Various Eosinophilic Esophagitis Therapies
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15. The BODY-Q Cellulite Scale: A Development and Validation Study
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16. Use of the Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND) in X-Linked Myotubular Myopathy: Content Validity and Psychometric Performance
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17. An international mixed methods study to develop a new preference-based measure for women with breast cancer: the BREAST-Q Utility module
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18. RETRACTED ARTICLE: Content validity and psychometric evaluation of Functional Assessment of Chronic Illness Therapy-Fatigue in patients with psoriatic arthritis
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19. Synergistic effect of moxibustion and rehabilitation training in functional recovery of post-stroke spastic hemiplegia
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20. The Patient Voice in Neovascular Age-Related Macular Degeneration: Findings from a Qualitative Study
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21. Validation of the Observer-Reported Communication Ability (ORCA) measure for individuals with Rett syndrome
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22. Content Validity of the Modified Functional Scale for the Assessment and Rating of Ataxia (f-SARA) Instrument in Spinocerebellar Ataxia
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23. Assessing Participants’ Experiences with Vitiligo from Patient Interviews
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24. Content evaluation of pruritus, skin pain and sleep disturbance patient-reported outcome measures for adolescents and adults with moderate-to-severe atopic dermatitis: qualitative interviews
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25. Symptoms and Functional Limitations in the First Year Following a Myocardial Infarction: A Qualitative Study
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26. The CDI-DaySyms: Content Development of a New Patient-Reported Outcome Questionnaire for Symptoms of Clostridium difficile Infection
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27. Evaluation of the psychometric properties of the Early Morning Symptoms of COPD Instrument (EMSCI)
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28. Patient-reported outcome (PRO) measure-based algorithm for clinical decision support in epilepsy outpatient follow-up: a test–retest reliability study
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29. Development of a patient‐reported outcomes symptom measure for patients with nontransfusion‐dependent thalassemia (NTDT‐PRO © )
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30. Development and Psychometric Validation of the BREAST-Q Animation Deformity Scale for Women Undergoing an Implant-Based Breast Reconstruction After Mastectomy
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31. Content validity of Scoliosis Research Society questionnaire-22 revised (SRS-22r) for adolescents with idiopathic scoliosis: protocol for a qualitative study exploring patient’s and practitioner’s perspectives
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32. Reliability and Validity of the Polish Version of the Esophageal-Atresia-Quality-of-Life Questionnaires to Assess Condition-Specific Quality of Life in Children and Adolescents Born with Esophageal Atresia
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33. Feasibility of Using Qualitative Interviews to Explore Patients’ Treatment Goals: Experience from Dermatology
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34. Development of a Questionnaire to Assess the Impact of Chronic Low Back Pain for Use in Regulated Clinical Trials
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35. Development and Content Validity of the Statin Experience Assessment Questionnaire (SEAQ)©
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36. Development and testing of candidate items for inclusion in a new rheumatoid arthritis stiffness patient-reported outcome measure
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37. Quality of life in coeliac disease: qualitative interviews to develop candidate items for the Coeliac Disease Assessment Questionnaire
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38. Acceptability of Patient-Reported Outcome and Experience Measures for Hepatitis C Treatment Among People Who Use Drugs
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39. Development and Psychometric Validation of BREAST-Q Scales Measuring Cancer Worry, Fatigue, and Impact on Work
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40. Place of patient-reported outcomes & experiences measurements (PROMS/PREMS) in the assessment and pricing of Health technologies in France
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41. Childhood esotropia: child and parent concerns
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42. Patient-reported outcome measure for neuromyelitis optica: pretesting of preliminary instrument and protocol for further development in accordance with international guidelines
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43. Editorial Commentary: Asking the Right Questions: Morbidity, Mortality, and Measuring What's Important in Unbiased Evaluations of Antimicrobials
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44. Everyday Barriers in Communicative Participation According to People With Communication Problems
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45. The Concizumab Pen-Injector is Easy to Use and Preferred by Hemophilia Patients and Caregivers: A Usability Study Assessing Pen-Injector Handling and Preference
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46. Patient-reported treatment-related symptom burden for patients with advanced melanoma in Canada
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47. An Evidence-Based, Nursing Handover Standard for a Multisite Public Hospital in Switzerland: Web-Based, Modified Delphi Study
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48. The Cystic Fibrosis Impact Questionnaire: qualitative development and cognitive evaluation of a new patient-reported outcome instrument to assess the life impacts of cystic fibrosis
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49. A Qualitative Study to Assess the Content Validity of the 24‐Hour Migraine Quality of Life Questionnaire in Patients with Migraine
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50. A structured review evaluating content validity of the Asthma Control Test, and its consistency with U.S. guidelines and patient expectations for asthma control
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51. Validation of the Dutch translation of the quality of recovery-15 scale
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52. A Patient-Centered Perspective of Molluscum Contagiosum as Reported by B-SIMPLE4 Clinical Trial Patients and Caregivers: Global Impression of Change and Exit Interview Substudy Results
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53. Content Validity of the Hypogonadism Impact of Symptoms Questionnaire (HIS-Q): A Patient-Reported Outcome Measure to Evaluate Symptoms of Hypogonadism
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54. A conceptual and disease model framework for osteoporotic kyphosis
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55. Financial Management Activity Process: Qualitative inquiry of adults with acquired brain injury
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56. The patient experience of Wilson disease: a conceptual model based on qualitative research
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57. A Mixed-Method Approach to Develop and Validate an Integrated Food Literacy Tool for Personalized Food Literacy Guidance
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58. Are treatment benefits in neuropathic pain reflected in the self assessment of treatment questionnaire?
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59. Responsiveness of SF-36 Health Survey and Patient Generated Index in people with chronic knee pain commenced on oral analgesia: analysis of data from a randomised controlled clinical trial
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60. Health‐related quality of life experiences in children and adolescents born with esophageal atresia: A Swedish–German focus group study
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61. A Systematic Method for Selecting Patient-Reported Outcome Measures in Diabetes Research
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62. Development of the neurotrophic keratopathy questionnaire: qualitative research
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63. Measuring the impact of burn injury on the parent-reported health outcomes of children 1-to-5 years: Item pool development for the Preschool1–5 Life Impact Burn Recovery Evaluation (LIBRE) Profile
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64. Development of the Multiple Myeloma Symptom and Impact Questionnaire: A New Patient-Reported Outcome Instrument to Assess Symptom and Impacts in Patients With Multiple Myeloma
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65. Patients’ Experiences With Staphylococcus aureus and Gram-Negative Bacterial Bloodstream Infections: Results From Cognitive Interviews to Inform Assessment of Health-Related Quality of Life
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66. China Health Related Outcomes Measures (CHROME): Development of a New Generic Preference-Based Measure for the Chinese Population
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67. Development of a disease conceptual model of patient experience with metastatic colorectal cancer: identification of the most salient symptoms and impacts
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68. Patient-reported outcome measurement in palliative care: A hermeneutic narrative review
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69. Experience of Daily Life with Generalized Myasthenia Gravis: A Qualitative Investigation and Assessment of Instrument Content Validity
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70. Care recipient self-perceived burden: Perspectives of individuals with chronic health conditions or personal experiences with caregiving on caregiver burden in the US
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71. Patient-Reported Outcome Measure Development and Validation: A Primer for Clinicians
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72. The development of the ICIQ‐UAB: A patient reported outcome measure for underactive bladder
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73. Health-Related Quality of Life in Focal Segmental Glomerular Sclerosis and Minimal Change Disease: A Qualitative Study of Children and Adults to Inform Patient-Reported Outcomes
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74. Development and Content Validity of the Physical Activity Questionnaire-Young Children (PAQ-YC) to Assess Physical Activity in Children between 5 and 7 Years
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75. A qualitative study of the impacts of having an infant or young child with achondroplasia on parent well-being
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76. A qualitative interview study to explore adolescents’ experience of alopecia areata and the content validity of sign/symptom patient‐reported outcome measures*
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77. Asthma Daytime Symptom Diary (ADSD) and Asthma Nighttime Symptom Diary (ANSD): Measurement Properties of Novel Patient-Reported Symptom Measures
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78. The patient-reported outcomes measurement information systems (PROMIS®) physical function and its derivative measures in adults: a systematic review of content validity
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79. Determining Severity Strata for Three Atopic Dermatitis Patient-Reported Outcome Questionnaires: Defining Severity Score Ranges for the Worst Pruritus Numerical Rating Scale and the Atopic Dermatitis Symptom and Impact Scales (ADerm-SS and ADerm-IS)
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80. Patient-Reported Outcome Measures in the Food and Drug Administration Pilot Compendium: Meeting Today’s Standards for Patient Engagement in Development?
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81. Developing fit-for-purpose self-report instruments for assessing consumer responses to tobacco and nicotine products: the ABOUT™ Toolbox initiative
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82. Identifying dimensions of fatigue in haemodialysis important to patients, caregivers and health professionals: An international survey
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83. Exploring what is important to patients with regards to quality of life after experiencing a lower limb reconstructive procedure: a qualitative evidence synthesis
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84. Measurement Properties of the Psoriasis Symptom Inventory Electronic Daily Diary in Patients with Moderate to Severe Plaque Psoriasis
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85. Developing an Evidence-Based Nursing Handover Standard for a Multi-Site Public Hospital in Switzerland: Protocol for a Web-Based, Modified Delphi Study
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86. Qualitative Research and Content Validity
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87. The power of words: evaluating the role of qualitative methods in cancer research
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88. Development of the Patient- and Observer-Reported PRUCISION Instruments to Assess Pruritus and Sleep Disturbance in Pediatric Patients with Cholestatic Liver Diseases
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89. Establishment of a condition-specific quality-of-life questionnaire for children born with esophageal atresia aged 2–7 across 14 countries
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90. Patient-Reported Outcome Measures Used in Randomized Controlled Trials Following Surgical Intervention for Endometriosis: A Structured Review from the AAGL Practice Guidelines Group
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91. A Narrative Review of Patient-Reported Outcome Measures and Their Application in Recent Pediatric Surgical Research: Advancing Knowledge and Offering New Perspectives to the Field
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92. Patient Experience of Treatment with Tirzepatide for Weight Management: Exit Interviews from SURMOUNT-4
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93. Health state utility values for metastatic pancreatic cancer using a composite time trade-off based on the vignette-based approach in Japan
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94. Health‐related quality of life and patient‐reported outcome measurements in patients with cystinosis
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