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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03888313
Other study ID # INFOM
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 26, 2019
Est. completion date January 13, 2021

Study information

Verified date January 2021
Source Sahlgrenska University Hospital, Sweden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

An explorative study of the patients' experience of participating at a group consultation, together with other patients with newly diagnosed colon or rectal cancer


Description:

The group consultation is planned to be on the Friday of the same week as the patient recieved a suggested treatment plan i.e. after MDT, at a personal consultation with his/her colorectal surgeon. During the group consultation the steps necessary for the patient to take responsability for in connection with the operation. Ample time for questions, clarifications and discussions. Appropriate clinical trials are presented


Recruitment information / eligibility

Status Completed
Enrollment 161
Est. completion date January 13, 2021
Est. primary completion date November 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 120 Years
Eligibility Inclusion Criteria: - Patients participating in the pretreatment group consultation Exclusion Criteria: - Not able to answer questionnaire

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Pretreatment group consultation
A consultation in group with several patients and one surgeon

Locations

Country Name City State
Sweden Sahlgrenska University Hospital/Östra Gothenburg Västra Götaland Region

Sponsors (1)

Lead Sponsor Collaborator
Sahlgrenska University Hospital, Sweden

Country where clinical trial is conducted

Sweden, 

References & Publications (1)

Walming S, Angenete E, Bock D, Block M, de la Croix H, Wedin A, Haglind E. Preoperative Group Consultation Prior to Surgery for Colorectal Cancer-an Explorative Study of a New Patient Education Method. J Cancer Educ. 2021 Jan 14. doi: 10.1007/s13187-020-0 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The patient's experience of participating in a pretreatment group consultation A questionnaire with questions on the patient's experience of the information received and their experience of participating in the pretreatment group consultation will be used to collect descriptive data. Some of the questions have been developed through semi-structured interviews with patients with colon or rectal cancer other are standardized questionnaires used in other studies.
The questionnaire includes questions on which information resources the patients have used (such as social media, patient organizations).Their experience of the pretreatment group consultation will be assessed by "Would you recommend someone in the same situation as you to attend the pretreatment group consultation?". Possible answering options are "Yes", "No" and "Don't know". The EuroQol's EQ-5D-5L for assessment of health related quality of will be included mainly as a tool for assurance of external validity, and not as an outcome measure. Both the indices and the VAS-scale may be used.
Before start of treatment
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