Kiran Pohar Manhas
Biographic Data
| ID | 5190088 |
|---|---|
| NAME | Kiran Pohar Manhas |
| GIVEN NAMES | Kiran Pohar |
| FAMILY NAME | Manhas |
| SIGNATURE | MANHAS K P |
| AFFILIATIONS | Alberta Health Services |
| ORCID | 0000-0002-1486-2387 |
| VERIFIED | Yes |
| TOTAL WORKS | 6 |
| TOTAL CITATIONS | 2 |
| WORKS AS AUTHOR | 6 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2014 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 1 |
A national atlas to improve the study of Canadians living with long Covid (post-Covid-19 condition)
Accessing Care Services for Long Covid Sufferers in Alberta, Canada
Designing appropriate rehabilitation programs for long COVID-19 remains challenging. The purpose of this study was to explore the patient experience of accessing long COVID-19 rehabilitation and recovery services. In this cross-sectional, observational study, a telephone survey was administered to a random sample of persons with long COVID-19 in a Canadian province. Participants included adults who tested positive for COVID-19 between March and O…
Exploring Rehabilitation Provider Experiences of Providing Health Services for People Living with Long Covid in Alberta
Provider experience of delivering long COVID care can be used to inform patient-centred service delivery for persons with long COVID symptoms
Exploring patient centredness, communication and shared decision‐making under a new model of care
Patient-centred care and patient engagement in healthcare and health research are widely mandated by funders, health systems and institutions. Increasingly, shared decision-making (SDM) is recognised as promoting patient-centred care. We explore this relationship by studying SDM in the context of integrating novel patient-centred policies in community rehabilitation. There is little research on SDM in rehabilitation, and less so in the critical c…
Parental perspectives on consent for participation in large-scale, non-biological data repositories
BACKGROUND: Data sharing presents several challenges to the informed consent process. Unique challenges emerge when sharing pediatric or pregnancy-related data. Here, parent preferences for sharing non-biological data are examined. METHODS: Groups (n = 4 groups, 18 participants) and individual interviews (n = 19 participants) were conducted with participants from two provincial, longitudinal pregnancy cohorts (AOB and APrON). Qualitative content …
Parent Perspectives on Privacy and Governance for a Pediatric Repository of Non-Biological, Research Data
Research data repositories (RDRs) are data storage entities where data can be submitted, stored, and subsequently accessed for purposes beyond the original intent. There is little information relating to non-biological RDRs, nor considerations regarding pediatric data storage and re-use. We examined parent perspectives on pediatric, non-biological RDRs. Qualitative, descriptive methods including both interviews and focus groups were used. Purposi…
Exploring patient centredness, communication and shared decision‐making under a new model of care
Patient-centred care and patient engagement in healthcare and health research are widely mandated by funders, health systems and institutions. Increasingly, shared decision-making (SDM) is recognised as promoting patient-centred care. We explore this relationship by studying SDM in the context of integrating novel patient-centred policies in community rehabilitation. There is little research on SDM in rehabilitation, and less so in the critical c…
Parent Perspectives on Privacy and Governance for a Pediatric Repository of Non-Biological, Research Data
Research data repositories (RDRs) are data storage entities where data can be submitted, stored, and subsequently accessed for purposes beyond the original intent. There is little information relating to non-biological RDRs, nor considerations regarding pediatric data storage and re-use. We examined parent perspectives on pediatric, non-biological RDRs. Qualitative, descriptive methods including both interviews and focus groups were used. Purposi…
Parent Perspectives on Privacy and Governance for a Pediatric Repository of Non-Biological, Research Data
Research data repositories (RDRs) are data storage entities where data can be submitted, stored, and subsequently accessed for purposes beyond the original intent. There is little information relating to non-biological RDRs, nor considerations regarding pediatric data storage and re-use. We examined parent perspectives on pediatric, non-biological RDRs. Qualitative, descriptive methods including both interviews and focus groups were used. Purposi…
Parental perspectives on consent for participation in large-scale, non-biological data repositories
BACKGROUND: Data sharing presents several challenges to the informed consent process. Unique challenges emerge when sharing pediatric or pregnancy-related data. Here, parent preferences for sharing non-biological data are examined. METHODS: Groups (n = 4 groups, 18 participants) and individual interviews (n = 19 participants) were conducted with participants from two provincial, longitudinal pregnancy cohorts (AOB and APrON). Qualitative content …
Exploring patient centredness, communication and shared decision‐making under a new model of care
Patient-centred care and patient engagement in healthcare and health research are widely mandated by funders, health systems and institutions. Increasingly, shared decision-making (SDM) is recognised as promoting patient-centred care. We explore this relationship by studying SDM in the context of integrating novel patient-centred policies in community rehabilitation. There is little research on SDM in rehabilitation, and less so in the critical c…
Accessing Care Services for Long Covid Sufferers in Alberta, Canada
Designing appropriate rehabilitation programs for long COVID-19 remains challenging. The purpose of this study was to explore the patient experience of accessing long COVID-19 rehabilitation and recovery services. In this cross-sectional, observational study, a telephone survey was administered to a random sample of persons with long COVID-19 in a Canadian province. Participants included adults who tested positive for COVID-19 between March and O…
Exploring Rehabilitation Provider Experiences of Providing Health Services for People Living with Long Covid in Alberta
Provider experience of delivering long COVID care can be used to inform patient-centred service delivery for persons with long COVID symptoms
A national atlas to improve the study of Canadians living with long Covid (post-Covid-19 condition)
Medicine (5 works) · Psychology (4 works) · Intensive Care Unit Cognitive Disorders (3 works) · Long-Term Effects of COVID-19 (3 works) · Political science (3 works) · Qualitative research (3 works) · Social Psychology (3 works) · Sociology (3 works) · 2019-20 coronavirus outbreak (2 works) · Business (2 works)