NCT01306344

Brief Summary

  1. 1.A qualitative descriptive design.
  2. 2.A phenomenologic approach to investigate the meaning of the ward round.
  3. 3.Interviews of patients, nurses and physicians.
  4. 4.A Master thesis.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
12

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Feb 2011

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2011

Completed
27 days until next milestone

First Submitted

Initial submission to the registry

February 28, 2011

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 1, 2011

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2011

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
Last Updated

March 1, 2011

Status Verified

February 1, 2011

Enrollment Period

28 days

First QC Date

February 28, 2011

Last Update Submit

February 28, 2011

Conditions

Teaching Rounds

Keywords

Qualitative ResearchInterview, PsychologicalPatientsNursesPhysicians

Study Arms (3)

Patients

Heterogeneous groups of patients (age, gender)

Nurses

Heterogeneous groups of nurses (age, gender, working experience)

Physicians

Heterogeneous groups of physicians (age, gender, working experience)

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Inpatients at a hospital ward. Nurses and physicians working at the same hospital ward. Heterogeneous groups.

You may qualify if:

  • Grown-ups, normal cognitive function, speaks norwegian.

You may not qualify if:

  • Children, vulnerable patientgroups, students.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Oslo University Hospital

Oslo, Norway

Location

Study Officials

  • Bjorg Christiansen, PhD

    Oslo University College

    STUDY DIRECTOR

Central Study Contacts

Sofia Olsen, Master

CONTACT

+4798646911sofiaols@broadpark.no

Bjorg Christiansen, PhD

CONTACT

+4722453738Bjorg.Christiansen@su.hio.no

Study Design

Study Type
observational
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 28, 2011

First Posted

March 1, 2011

Study Start

February 1, 2011

Primary Completion

March 1, 2011

Study Completion

December 1, 2011

Last Updated

March 1, 2011

Record last verified: 2011-02

Locations

NO(1)