Skip to main content
Clinical Trials/NCT05700929
NCT05700929
Active, Not Recruiting
N/A

Evaluation of a Patient-centered Communication Skills Training for Nursing Professionals in Germany: A Randomized Controlled Trail

Universitätsklinikum Hamburg-Eppendorf1 site in 1 country207 target enrollmentNovember 14, 2022
ConditionsCommunication

Overview

Phase
N/A
Intervention
Not specified
Conditions
Communication
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Enrollment
207
Locations
1
Primary Endpoint
Self-efficacy regarding communication with patients
Status
Active, Not Recruiting
Last Updated
last year

Overview

Brief Summary

The KOMPAT study aims to evaluate the effectiveness and feasibility of a needs-based communication skills training for nursing professionals in Germany and to derive recommendations for future long-term implementation. Therefore, a training program to foster communication skills of nursing professionals has been developed based on a previously conducted needs assessment and literature research. To evaluate the training a randomized controlled trail with a waitlist-control group will be conducted. It is aimed to include 180 nurses within the study, of which 90 nurse will be randomized in a stratified manner to the intervention group and 90 nurses will be randomized to the waitlist-control group. Outcomes will be assessed at baseline, post -training and 4-weeks follow-up. It is hypothesized that self-efficacy in communication with patients and further outcomes will be significantly higher among participants in the intervention group compared to participants of the waitlist-control group during post-training assessment and follow-up. The evaluation will be accompanied by a process evaluation. The training will be facilitated by a member of the research team and a nursing professional by applying the train-the-trainer approach. The KOMPAT study will be conducted at the University Medical Center Hamburg-Eppendorf.

Registry
clinicaltrials.gov
Start Date
November 14, 2022
End Date
November 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Isabelle Scholl

Prof.Dr.

Universitätsklinikum Hamburg-Eppendorf

Eligibility Criteria

Inclusion Criteria

  • Nurses working at the participating departments of the University Medical Center Hamburg-Eppendorf
  • Main part of daily work includes communication with patients
  • Age ≥ 18 years
  • Completed educational program as a nurse
  • German-speaking

Exclusion Criteria

  • Little or no contact with patients in daily work, e.g. an operating room nurse or within the bed management

Outcomes

Primary Outcomes

Self-efficacy regarding communication with patients

Time Frame: Change from baseline (t0) at immediately after the training (t1) (with t1 being the primary endpoint) and at four weeks after the training (t2) for the intervention and waitlist-control group.

Description: Self-efficacy of nurses in the context of communication with their patients will be measured by the German version of the 12-item Self-Efficacy Scale (SE-12-G). Items on this one-dimensional scale can be answered on a scale from 1 ("very uncertain") to 10 ("very certain") with an additional option to rate items as "not relevant".

Secondary Outcomes

  • Objective knowledge about patient-centered communication(Change from baseline (t0) at immediately after the training (t1) and at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Attitudes towards medical communication(Change from baseline (t0) at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Subjective knowledge about patient-centered communication(Change from baseline (t0) at immediately after the training (t1) and at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Depression and anxiety(Change from baseline (t0) at immediately after the training (t1) and at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Rating of the training(immediately after the training (t1) for the intervention group)
  • Communication skills of nurses from simulation patients' perspective after participation in a SPA(four weeks after the training (t2) for the intervention and waitlist-control group)
  • Experienced patient-centeredness (Covariate)(Change from baseline (t0) at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Impact of contamination (Covariate)(for the intervention group at baseline (t0) only; for the waitlist-control group at baseline (t0), immediately after the training (t1) and four weeks after the training (t2))
  • Communication skills of nurses from external observers' perspective after participation in a SPA(four weeks after the training (t2) for the intervention and waitlist-control group)
  • Self-assessed communication skills from participants' perspective after participation in a SPA(four weeks after the training (t2) for the intervention and waitlist-control group)
  • Professional fulfillment(Change from baseline (t0) at immediately after the training (t1) and at four weeks after the training (t2) for the intervention and waitlist-control group)
  • Subjective working capacities(Change from baseline (t0) at immediately after the training (t1) and at four weeks after the training (t2) for the intervention and waitlist-control group)

Study Sites (1)

Loading locations...

Similar Trials