PubRank

Pragmatic Implementation Trial of a CF Primary Palliative Care Intervention

Clinical Trial ID NCT04923880

PubWeight™ 0.00‹?›

🔗 Visit the ClinicalTrials.gov page for NCT04923880

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A global measure of perceived stress. J Health Soc Behav 1983 56.90
2 Validation and utility of a self-report version of PRIME-MD: the PHQ primary care study. Primary Care Evaluation of Mental Disorders. Patient Health Questionnaire. JAMA 1999 40.00
3 A brief measure for assessing generalized anxiety disorder: the GAD-7. Arch Intern Med 2006 21.56
4 The PHQ-8 as a measure of current depression in the general population. J Affect Disord 2008 8.49
5 A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006 5.74
6 Monitoring depression treatment outcomes with the patient health questionnaire-9. Med Care 2004 4.92
7 Generalist plus specialist palliative care--creating a more sustainable model. N Engl J Med 2013 4.27
8 Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items. Qual Life Res 2009 4.13
9 Prevalence of depression and anxiety in patients with cystic fibrosis and parent caregivers: results of The International Depression Epidemiological Study across nine countries. Thorax 2014 2.87
10 Determination of the minimal clinically important difference scores for the Cystic Fibrosis Questionnaire-Revised respiratory symptom scale in two populations of patients with cystic fibrosis and chronic Pseudomonas aeruginosa airway infection. Chest 2009 2.43
11 Validation of a disease-specific measure of health-related quality of life for children with cystic fibrosis. J Pediatr Psychol 2003 2.14
12 The measurement of symptoms in children with cancer. J Pain Symptom Manage 2000 1.85
13 The measurement of symptoms in young children with cancer: the validation of the Memorial Symptom Assessment Scale in children aged 7-12. J Pain Symptom Manage 2002 1.36
14 Development of six PROMIS pediatrics proxy-report item banks. Health Qual Life Outcomes 2012 1.29
15 Impact of socioeconomic status, race, and ethnicity on quality of life in patients with cystic fibrosis in the United States. Chest 2009 1.11
16 Self-reported physical and psychological symptom burden in adults with cystic fibrosis. J Pain Symptom Manage 2008 1.05
17 Assessing stress in cancer patients: a second-order factor analysis model for the Perceived Stress Scale. Assessment 2004 1.05
18 Erratum to: Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national, US sample. Qual Life Res 2012 0.93
19 Item banks for alcohol use from the Patient-Reported Outcomes Measurement Information System (PROMIS): use, consequences, and expectancies. Drug Alcohol Depend 2012 0.89
20 Initial evaluation of the Parent Cystic Fibrosis Questionnaire--Revised (CFQ-R) in infants and young children. J Cyst Fibros 2014 0.80
21 Development of a brief assessment scale for caregivers of the medically ill. J Pain Symptom Manage 2005 0.78
22 A Systematic Review of the Use of the Palliative Care Outcome Scale and the Support Team Assessment Schedule in Palliative Care. J Pain Symptom Manage 2015 0.77
23 Screening for ADHD in adults with cystic fibrosis: Prevalence, health-related quality of life, and adherence. J Cyst Fibros 2017 0.75
24 Trajectories of caregiver burden in families of adult cystic fibrosis patients. Palliat Support Care 2017 0.75
25 Web-based symptom screening in cystic fibrosis patients: A feasibility study. J Cyst Fibros 2015 0.75
26 The CF-CARES primary palliative care model: A CF-specific structured assessment of symptoms, distress, and coping. J Cyst Fibros 2017 0.75
27 Development and evaluation of a palliative care curriculum for cystic fibrosis healthcare providers. J Cyst Fibros 2015 0.75
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