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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00750672
Other study ID # OHRI 2008-361
Secondary ID 2008361-01H for
Status Completed
Phase N/A
First received September 9, 2008
Last updated July 11, 2012
Start date August 2008
Est. completion date February 2010

Study information

Verified date July 2012
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Observational

Clinical Trial Summary

The purposes of this study are to examine the needs (symptoms, support, information) and satisfaction of women during follow-up in the community after completing treatment for endometrial cancer. This information will be collected from the perspective of the women themselves, their primary care providers (family physician or gynecologist) and the health care providers (oncologist, nurses, social worker, psychologist) at the cancer centre.


Description:

Research Question How has this transfer in follow-up care impacted performance indicators?

- Volume of follow-up care transferred

- Percentage of women, who have required a re-entry consultation

- Fiscal implication of this transfer of follow-up care

Patient stakeholders:

- What are women's perceptions of the transition of follow-up care?

- What are women's supportive care needs during the transition of follow-up care and ongoing needs?

Primary Care Practitioner stakeholders:

- What are the primary care practitioners' perceptions of the process of transition of follow-up care?

- What are the primary care practitioners' educational needs?

- What are the primary care practitioners' perceptions of the process of re-entry for in women with suspected recurrence?

Tertiary Centre: Health care providers stakeholders

o What are the perceptions of tertiary health care providers about the transition of follow-up care?


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date February 2010
Est. primary completion date September 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Participants- women diagnosed with endometrial cancer:

- 18 years of age or older.

- speak English or French

- who have been treated (surgery and/or radiation therapy) at TOH.

- who have been discharged from follow-up in the cancer centre in the past 6 months.

- Participants-primary care provider practitioner:

- providing follow-up care to at least one woman with endometrial cancer

- Participants- health care providers at the tertiary centre :

- physicians, nurses or allied health care providers whose primary responsibility are to provide care to women with gynecological cancer.

Exclusion Criteria:

Study Design

Observational Model: Ecologic or Community, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada The Ottawa Hospital Ottawa Ontario

Sponsors (2)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute Ottawa Regional Cancer Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Qualitative description of participants perception after 6 month No
See also
  Status Clinical Trial Phase
Recruiting NCT02822833 - The Role of Indocyanine Green to Identify Sentinel Lymph Node in Uterine Cancer N/A