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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03654950
Other study ID # PEPP
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2018
Est. completion date December 1, 2021

Study information

Verified date November 2022
Source Sahlgrenska University Hospital, Sweden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The overall aim with this study is to gain a deeper understanding of patient perceptions regarding empowerment in relation to a health platform.


Description:

This is a two-stage study design. The first stage consists of focus groups interviews. Three focus groups with 6-8 patients (colorectal cancer patients diagnosed at least one year ago) in each group, will be invited. The focus group interviews will be moderated by one researcher, but accompanied with a second observing researcher. The participants will be identified using the regional Swedish ColoRectal Cancer Registry in Västra Götaland. The participants will be contacted by a short letter (appendix) indicating that we will call them with more information. The participants will by phone be asked to participate in the study and then invited to the focus groups. The second phase of the project includes a questionnaire, which will be sent to 200 patients from the same population. The questionnaires will be delivered by using the Sunet Survey system, which is a system approved by University of Gothenburg. If the participants prefers a paper copy, or lack the possibility to reply online, a paper copy will be send via mail instead. At this moment the investigators have developed a questionnaire, which may be refined due to the understating achieved from the focus group interviews.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient with colorectal cancer Exclusion Criteria: - Inability to give informed consent or speaking and reading the Swedish language.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
Interviews and questionnaires

Locations

Country Name City State
Sweden Dept. of Surgery, Sahlgrenska University Hospital/Ostra Gothenburg

Sponsors (2)

Lead Sponsor Collaborator
Sahlgrenska University Hospital, Sweden Högskolan Väst

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient reported experiences in themes interview 1 day
Secondary Patient reported experiences divided into themes Interview 12 months
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