Information Needs After Surgery for Colorectal Cancer
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Purpose
Aim The overall aim was to investigate information needs after surgery for colorectal cancer and factors explaining information needs, both from the patients' perspective and the next of kin's.
| Condition |
|---|
|
Colorectal Cancer |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Information Needs After Surgery for Colorectal Cancer - From the Perspective of the Patient and Next of Kin |
- Information needs - patients' and next of kins' [ Time Frame: 7 weeks ] [ Designated as safety issue: No ]In the interviews with patients and next of kins separately they are asked to express their needs for information at that time.
| Enrollment: | 100 |
| Study Start Date: | January 2007 |
| Study Completion Date: | August 2009 |
| Primary Completion Date: | August 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Surgery for colorectal cancer
Patients that had surgery for colorectal cancer without receiving a stoma, and their next of kin.
|
Detailed Description:
Sample Inclusion criteria are patients over 18 years of age that have gone through a surgery for colorectal cancer without having a stoma, and their next of kin with whom they live.
Instruments In study I, 100 patients filled in four different instruments 1-2 weeks after discharge to measure: QOL, information needs, sense of coherence and performance status.
QLQ-C30 and QLQ-CR38 were used to measure QOL. INFO26 were used to measure received information. The SOC - Sense of Coherence was used to measure sense of coherence. And finally the scale for ECOG Performance Status was used to measure the level of physical performance status.
In study II the same patients filled in the same instruments a second time, 5-7 week after discharge.
Information about marital status, occupation, diagnosis and prognosis were taken from the medical record.
Interviews In study III 16 patients both filled in the instruments in study I and II, and were interviewed to gain a deeper understanding of their information needs. The interviews were semi structured and will be analysed with content analysis.
In study IV the next of kin to patients in study III were interviewed about their own information needs in connection to discharge.
The interviews were performed twice for each person, 1-2 weeks after discharge and a second time, 5-7 week after discharge.
Data sampling The data were collected consecutively, and every third patient living together with their next of kin were asked to participate in the interviews.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Inclusion criteria are patients over 18 years of age that have had a surgery for colorectal cancer without having a stoma, and their next of kin with whom they live. They should be able to speak and read Swedish.
Inclusion Criteria:
- adult over 18 years of age
- surgery for colorectal cancer in one of the three hospitals in the study
- speak and read Swedish
- be able to understand the instructions written in the questionnaires
Exclusion Criteria:
- receiving a stoma
- don't want to participate
- not completed at least half of the items in both questionnaires
Contacts and Locations| Sweden | |
| Surgical clinic | |
| Helsingborg, Skåne, Sweden, 25187 | |
| Surgical clinic | |
| Lund, Skåne, Sweden, 22185 | |
| Surgical clinic | |
| Malmö, Skåne, Sweden, 20502 | |
| Principal Investigator: | Maria Lithner, RN | Surgical clinic, Lund, Sweden |
More Information
No publications provided
| Responsible Party: | Jan Johansson, MD, Associate professor, Dpt of Surgery, Lund University, Sweden |
| ClinicalTrials.gov Identifier: | NCT01303393 History of Changes |
| Other Study ID Numbers: | Etics review Dnr 558/2006 |
| Study First Received: | February 23, 2011 |
| Last Updated: | February 23, 2011 |
| Health Authority: | Sweden: The National Board of Health and Welfare |
Keywords provided by Region Skane:
|
Patient education. Patient discharge. Needs assessment. |
Additional relevant MeSH terms:
|
Colorectal Neoplasms Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms |
Digestive System Diseases Gastrointestinal Diseases Colonic Diseases Intestinal Diseases Rectal Diseases |
ClinicalTrials.gov processed this record on May 22, 2013