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Completed

NCT Number: NCT01303393

Information Needs After Surgery for Colorectal Cancer

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Surgical clinic, Helsingborg, Skåne County, Sweden

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Secondary outcomes

  1. Information needs - patients' and next of kins'

    Time frame: 7 weeks

    In the interviews with patients and next of kins separately they are asked to express their needs for information at that time.

Sponsors and collaborators

Lead sponsor

Region Skane

Other

Collaborators

  • Lund University

Registry information

Official study title

Information Needs After Surgery for Colorectal Cancer - From the Perspective of the Patient and Next of Kin

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Feb 24, 2011
Registry last updated
Feb 24, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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