Pamela S Hinds
Biographic Data
| ID | 285988 |
|---|---|
| NAME | Pamela S Hinds |
| GIVEN NAMES | Pamela S |
| FAMILY NAME | Hinds |
| SIGNATURE | HINDS P S |
| AFFILIATIONS | Children's National |
| ORCID | 0000-0001-6491-6649 |
| VERIFIED | Yes |
| TOTAL WORKS | 18 |
| TOTAL CITATIONS | 67 |
| AUTHOR COUNT | 18 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 1992 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 3 |
Profiles of quality of life among US young adult cancer survivors and their associations with potential psychosocial intervention targets of hope and psychological flexibility
Honoring the Good Parent Intentions of Courageous Parents: A Thematic Summary from a US-Based National Survey
Familiarity with parental perspectives on their parenting goodness and goals is a necessary core of family-centric health care
The association of age, literacy, and race on completing patient-reported outcome measures in pediatric oncology
Life after loss: Parent bereavement and coping experiences after infant death in the neonatal intensive care unit
The death of an infant in the neonatal intensive care unit (NICU) is a profound and unexpected loss for parents that results in a complex process of coping with bereavement. A descriptive qualitative approach was used to explore parent bereavement and coping experiences after infant death in the NICU. The dual process model of coping with bereavement was used as a conceptual framework to help understand how parents cope with grief after infant de…
A randomized clinical trial of adolescents with HIV/Aids: Pediatric advance care planning
The objective of this study is to determine if pediatric advance care planning (pACP) increases adolescent/family congruence in end-of-life (EOL) treatment preferences longitudinally. Adolescents aged 14-21 years with HIV/AIDS and their families were randomized (N = 105 dyads) to three-60-minute sessions scheduled one week apart: either the pACP intervention (survey administered independently, facilitated conversation with adolescent and family p…
Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease
Comparability of the Patient-Reported Outcomes Measurement Information System Pediatric short form symptom measures across culture: Examination between Chinese and American children with cancer
PROMIS® pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions
Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method
The emotional distress of children with cancer in China: An item response analysis of C-Ped-PROMIS Anxiety and Depression short forms
Isoqol recommends minimum standards for patient-reported outcome measures used in patient-centered outcomes and comparative effectiveness research
Comparing longitudinal assessments of quality of life by patient and parent in newly diagnosed children with cancer: The value of both raters’ perspectives
Response to the Commentary by Furlong & Barr on Cox CL, Lensing S, Rai SN et al: Proxy assessment of quality of life in pediatric trials: Application of the Health Utilities Index 3
Proxy assessment of quality of life in pediatric clinical trials: Application of the Health Utilities Index 3
Quality of life as conveyed by pediatric patients with cancer
Human-robot Interaction: A Special Double Issue of Human-Computer Interaction
This special issue is made up of five articles which cover the emerging area of human-robot interaction. The first paper offers a theoretical ecological framework for the design of personal service robots in homes of elderly people. Next, a field study of two robots that visited a children's elementary school in Japan for two weeks, with the purpos
The Possibilities and Pitfalls of Doing a Secondary Analysis of a Qualitative Data Set
The purpose of this article is to identify the general methodologic and data set-specific challenges that must be overcome when attempting a secondary analysis of qualitative data. Two separate examples of secondary analyses of qualitative data sets are also described, including one unsuccessful beginning
Context as a Source of Meaning and Understanding
The intent of health professions is to understand humans, their health, and other related phenomena and to use this understanding to promote meaningful life experiences. The ability to do this depends on knowledge of the multiple contexts in which these phenomena exist. The purposeful use of context is a central feature of thorough research and clinical assessments, and it allows for meaning to be shared and phenomena to be understood. This artic…
The Possibilities and Pitfalls of Doing a Secondary Analysis of a Qualitative Data Set
The purpose of this article is to identify the general methodologic and data set-specific challenges that must be overcome when attempting a secondary analysis of qualitative data. Two separate examples of secondary analyses of qualitative data sets are also described, including one unsuccessful beginning
Context as a Source of Meaning and Understanding
The intent of health professions is to understand humans, their health, and other related phenomena and to use this understanding to promote meaningful life experiences. The ability to do this depends on knowledge of the multiple contexts in which these phenomena exist. The purposeful use of context is a central feature of thorough research and clinical assessments, and it allows for meaning to be shared and phenomena to be understood. This artic…
Life after loss: Parent bereavement and coping experiences after infant death in the neonatal intensive care unit
The death of an infant in the neonatal intensive care unit (NICU) is a profound and unexpected loss for parents that results in a complex process of coping with bereavement. A descriptive qualitative approach was used to explore parent bereavement and coping experiences after infant death in the NICU. The dual process model of coping with bereavement was used as a conceptual framework to help understand how parents cope with grief after infant de…
Human-robot Interaction: A Special Double Issue of Human-Computer Interaction
This special issue is made up of five articles which cover the emerging area of human-robot interaction. The first paper offers a theoretical ecological framework for the design of personal service robots in homes of elderly people. Next, a field study of two robots that visited a children's elementary school in Japan for two weeks, with the purpos
Context as a Source of Meaning and Understanding
The intent of health professions is to understand humans, their health, and other related phenomena and to use this understanding to promote meaningful life experiences. The ability to do this depends on knowledge of the multiple contexts in which these phenomena exist. The purposeful use of context is a central feature of thorough research and clinical assessments, and it allows for meaning to be shared and phenomena to be understood. This artic…
The Possibilities and Pitfalls of Doing a Secondary Analysis of a Qualitative Data Set
The purpose of this article is to identify the general methodologic and data set-specific challenges that must be overcome when attempting a secondary analysis of qualitative data. Two separate examples of secondary analyses of qualitative data sets are also described, including one unsuccessful beginning
Quality of life as conveyed by pediatric patients with cancer
Human-robot Interaction: A Special Double Issue of Human-Computer Interaction
This special issue is made up of five articles which cover the emerging area of human-robot interaction. The first paper offers a theoretical ecological framework for the design of personal service robots in homes of elderly people. Next, a field study of two robots that visited a children's elementary school in Japan for two weeks, with the purpos
Proxy assessment of quality of life in pediatric clinical trials: Application of the Health Utilities Index 3
Response to the Commentary by Furlong & Barr on Cox CL, Lensing S, Rai SN et al: Proxy assessment of quality of life in pediatric trials: Application of the Health Utilities Index 3
Comparing longitudinal assessments of quality of life by patient and parent in newly diagnosed children with cancer: The value of both raters’ perspectives
Isoqol recommends minimum standards for patient-reported outcome measures used in patient-centered outcomes and comparative effectiveness research
The emotional distress of children with cancer in China: An item response analysis of C-Ped-PROMIS Anxiety and Depression short forms
PROMIS® pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions
Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method
Comparability of the Patient-Reported Outcomes Measurement Information System Pediatric short form symptom measures across culture: Examination between Chinese and American children with cancer
A randomized clinical trial of adolescents with HIV/Aids: Pediatric advance care planning
The objective of this study is to determine if pediatric advance care planning (pACP) increases adolescent/family congruence in end-of-life (EOL) treatment preferences longitudinally. Adolescents aged 14-21 years with HIV/AIDS and their families were randomized (N = 105 dyads) to three-60-minute sessions scheduled one week apart: either the pACP intervention (survey administered independently, facilitated conversation with adolescent and family p…
Assessing responsiveness over time of the PROMIS® pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease
Life after loss: Parent bereavement and coping experiences after infant death in the neonatal intensive care unit
The death of an infant in the neonatal intensive care unit (NICU) is a profound and unexpected loss for parents that results in a complex process of coping with bereavement. A descriptive qualitative approach was used to explore parent bereavement and coping experiences after infant death in the NICU. The dual process model of coping with bereavement was used as a conceptual framework to help understand how parents cope with grief after infant de…
The association of age, literacy, and race on completing patient-reported outcome measures in pediatric oncology
Honoring the Good Parent Intentions of Courageous Parents: A Thematic Summary from a US-Based National Survey
Familiarity with parental perspectives on their parenting goodness and goals is a necessary core of family-centric health care
Profiles of quality of life among US young adult cancer survivors and their associations with potential psychosocial intervention targets of hope and psychological flexibility
Childhood Cancer Survivors' Quality of Life (13 works) · Medicine (13 works) · Psychology (12 works) · Public health (10 works) · Clinical Psychology (9 works) · Clinical Psychology (9 works) · Quality of Life Research (9 works) · Internal Medicine (6 works) · Cancer (5 works) · Pathology (5 works)