Feasibility of the Post-Stroke Depression-toolkit

April 9, 2018 updated by: Dr. Mariska van Dijk, University of Applied Sciences Utrecht

Feasibility of a Nurse-led Intervention for the Early Management of Depression After Stroke in Hospital

Rationale: Depression is a frequent complication after a stroke. In stroke guidelines several recommendations focus on early screening, and treatment off depression after stroke. Introducing clinical practice guidelines into routine daily practice however, is a difficult process. In order to make the recommendations applicable to clinical practice a toolkit was developed (the Post Stroke Depression-toolkit), which provides assessment tools for the early detection of depression after stroke, and a set of interventions in case of a positive screening for (risk on) depressive symptoms.

Objective: to investigate the feasibility of the Post Stroke Depression-toolkit in daily practice.

Study design: An explanatory mixed-methods, before-and-after study design. Study population: Nurses working on the neurological wards of one university hospital and two general hospitals in the Netherlands were included in the study. Additionally, data were obtained from patient charts.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Worldwide, approximately 50 million people who survived a stroke cope with physical, cognitive, and emotional impairments, and many of these survivors depend on caregivers to manage activities of daily living (Miller, et al., 2010). Stroke is the third leading cause of disability (Johnson, et al., 2016). Depression is a frequent and serious complication after stroke impeding rehabilitation outcome, and is associated with a higher mortality risk, and a lower quality of life (Kutlubaev & Hackett, 2014; Robinson & Jorge, 2015).

There is growing evidence for successful treatment of depression after stroke (Robinson & Jorge, 2015). Recommendations of stroke guidelines on the early management of depressive symptoms have not been structurally implemented in current practice, and only a minority of the acute care stroke teams assess mood on a systematic way in daily care (Hart & Bowen, 2008; Bowen, et al., 2005). Hence, depression is still one of the most underdiagnosed and undertreated complications after stroke (Miller et al., 2010), resulting in worse patient outcomes and delayed recovery (Robinson & Jorge, 2015). In a feasibility study of the Nursing Rehabilitation Guideline for Stroke (Hafsteinsdóttir & Schuurmans, 2009) it was suggested that simplifying the guideline and integrating the recommendations into a stroke care pathway could gain a more positive attitude towards the guideline and improve its feasibility (Hafsteinsdóttir et al., 2013). Therefore, the Post-Stroke Depression toolkit (PSD toolkit), an intervention for the early management of depression after stroke, has been developed.

The feasibility of this intervention was tested following phase two of the British Medical Research Council (MRC) guidelines (Craig et al., 2013). In this study, feasibility (Polit & Beck, 2008) is measured in terms of (1) fidelity, defined as the extent to which the components of the PSD toolkit are delivered as intended, and (2) acceptability, defined as whether the PSD toolkit is judged suitable and satisfactory by the nurses (Gearing et al., 2011). After evaluating implementation, the sustainability of the PSD toolkit requires evaluation as well (Scheirer, 2005). Sustainability is defined as fidelity to the PSD toolkit six months after completing implementation.

The aims of the study were (1) to explore the feasibility of the PSD toolkit in terms of fidelity and acceptability in three phases-a pre-implementation phase, an implementation phase, and a sustainability phase six month after-and (2) to identify elements for further refinement and improvement in the toolkit to enhance its feasibility in daily stroke care during the hospital stay.

Design: An explanatory mixed-methods, before-and-after study design(Creswell, 2008).

Data were collected by patient chart audits and surveys among nurses. Individual and focus group interviews with nurses followed the quantitative data collection to explain the findings (Creswell, 2008).

Data were collected pre-implementation in March and April 2012, during implementation from April 2012 until December 2012 and during the sustainability phase from December 2012 until June 2013.

A team with expertise in stroke care, consisting of two researchers and five nurses from the participating nursing teams, guided the implementation.

Participants and setting Nurses working on the neurological wards of one university hospital and two general hospitals in the Netherlands were included in the study. Additionally, data were obtained from patient charts.

Implementation strategies Evidence-based implementation strategies were used to facilitate the implementation of the PSD toolkit: (1) education and training of the nurses in applying the PSD toolkit, (2) opinion leaders, and (3) audit and feedback by the researcher (Van Achterberg et al., 2008).

Data collection Baseline data To gain insight into the patients in whom the toolkit was used, data on gender, age, marital status, living arrangements, type of stroke, length of hospital stay, and discharge destination were collected. The demographics collected on the nurses included gender, age, education, years working on the ward, and full-time equivalent.

Patient chart audit Fidelity was measured in terms of the extent to which the components of the PSD toolkit were applied as intended; patient chart audits were performed to establish the number of patients who were screened for depressive symptoms and who received nursing interventions in the case of a positive screening.

The Barriers and Facilitators Assessment Instrument To obtain a thorough understanding of the experiences and opinions of the nurses that influence fidelity, perceived barriers were evaluated using the Barriers and Facilitators Assessment Instrument (BFAI) (Peters et al., 2002)consisting of 18 statements, both positively and negatively formulated. One of the authors of the original questionnaire reviewed and approved the adaptations, confirming the content validity. The nurses indicated, on a five-point Likert scale, if they (dis)agreed with a statement. The scale ranged from 5 (strongly agree) to 1 (strongly disagree). To identify barriers, the percentage who agreed and strongly agreed with the positively formulated statements were recoded into disagree and strongly disagree; an item score of >3 (agree/strongly agree) indicating a barrier.

The Clinical Utility Questionnaire Acceptability was measured in terms of the clinical utility (Harris & Warren, 1995) of the PSD toolkit as perceived by the nurses. Clinical utility was assessed using an adapted version of the Clinical Utility Questionnaire including 19 items addressing nurses' views on the toolkit, focussing on item clarity, acceptability of time investment, utility of the instruments, and relevance and utility of the nursing interventions. The content validity of the adapted questionnaire was assessed by one of the authors of the original questionnaire (de Man-van Ginkel et al., 2012).

Interviews with nurses To explain the results of the audits, BFAI and the Clinical Utility Questionnaire, semi-structured with the nurses on the participating wards were performed at the end of the implementation phase and three focus group interviews were conducted at the end of the sustainability phase. The interview guides consisted of the following topics derived from results of the audits and questionnaires: (1) presentation of the quantitative results, (2) possible explanations for the changes (decrease/increase) in fidelity, (3) nurses' views on barriers or facilitators to use of the PSD toolkit and its clinical utility, and (4) suggestions to further improve the toolkit.

Procedure Pre-implementation phase Data was collected on daily nursing care regarding the management of depressive symptoms after stroke. The researchers examined the charts of all patients admitted to the participating wards using a data extraction form.

Furthermore, all nurses and nursing students received education and training sessions totalling three hours, which covered (1) depression after stroke (causes, consequences, and the importance of early detection of depressive symptoms), evidence-based nursing interventions, and (2) the content and procedures of the PSD toolkit.

Implementation phase The researcher visited the participating wards four times per week for patient chart audits to collect baseline data and data on fidelity of the PSD toolkit by registering the frequency of delivery of the components of the PSD toolkit by the nurses. The researchers sent the results of the patient chart audit (e.g., the proportion of patients who were screened for depressive symptoms and who received nursing interventions) to the opinion leaders. Subsequently, the opinion leaders used this overview to provide feedback and to remind the nurses to screen a patient for depressive symptoms and apply appropriate nursing interventions.

At the end of the implementation phase, the researchers sent the BFAI and Clinical Utility Questionnaire to the nurses. After two weeks, a reminder was sent to all non-respondents. Subsequently, the researchers conducted individual interviews with a random sample of five nurses from each of the participating nursing teams to explain fidelity to and acceptability of the toolkit by discussing the outcomes of the audit, the BFAI and the Clinical Utility Questionnaire.

Sustainability phase During the sustainability phase, the same procedure was used as in the implementation phase; however, no implementation strategies, such as feedback and reminders, were used by the opinion leaders. At the end of the sustainability phase, three explanatory focus group interviews (one with each team, consisting of 10, 12 and 6 participants) were conducted with a randomly selected group of nurses to explain the data on fidelity to and acceptability of the PSD toolkit. The focus group interviews were moderated by a researcher who was not involved in implementation. The researchers and the research assistants observed, took notes, and handled the recording devices.

Data analysis

  • the baseline data, the audit data, and the results of the BFAI and Clinical Utility Questionnaire: Frequencies, means, standard deviations and percentages
  • comparison of differences in patient groups: the Chi-square test for categorical baseline data and t-tests
  • BFAI: numbers with the corresponding percentage of nurses who agreed and strongly agreed with an item on the questionnaire.
  • the Clinical Utility Questionnaire: a percentage of agreement with each item.

A change of +/-10% in fidelity and acceptability was used to indicate an increase or decrease (McCluskey & Middleton, 2010). SPSS, version 23 (SPSS Inc., Chicago, IL, USA) was used for quantitative data analysis.

The individual and focus group interviews with the nurses were analysed according to predefined codes based on the topics in the interview guides. All interviews, as well as the focus groups, were audiotaped and transcribed verbatim. The transcripts were studied, and initial items were identified by a researcher, and subsequently, the items were discussed between two researchers. Based on consensus, the final items that explained the quantitative results on fidelity and acceptability of the PSD toolkit were established.

Ethical considerations This study received ethics approval from the Medical Ethics Committee of a University Medical Center (12-081C) and the local medical ethics committees of the participating hospitals. Informed consent was obtained from all participants.

Study Type

Observational

Enrollment (Actual)

120

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All nurses working on the neurological wards and stroke units of the participating hospitals, one university hospital and two general hospitals.

Description

Inclusion Criteria:

  • Registered Nurses with or without Bachelor degree in Nursing (BN); Nursing students.

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Nurses
Nurses working on the neurological wards of three hospitals (one university hospital and two general hospitals)
Other: Post-Stroke Depression toolkit
The Post-Stroke Depression toolkit consists of three components: (1) two screening instruments, (2) seven evidence-based nursing interventions, and (3) an instruction manual.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Fidelity
Time Frame: 12 months
the extent to which the components of the PSD toolkit are delivered as intended
12 months
Acceptability
Time Frame: T=0; T=1 (after 6 months); T=2 (after 12 months)
whether the PSD toolkit is judged suitable and satisfactory by the nurses
T=0; T=1 (after 6 months); T=2 (after 12 months)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Applied Sciences Utrecht

Collaborators

UMC Utrecht

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 1, 2012

Primary Completion (ACTUAL)

June 30, 2013

Study Completion (ACTUAL)

June 30, 2013

Study Registration Dates

First Submitted

April 9, 2018

First Submitted That Met QC Criteria

April 9, 2018

First Posted (ACTUAL)

April 18, 2018

Study Record Updates

Last Update Posted (ACTUAL)

April 18, 2018

Last Update Submitted That Met QC Criteria

April 9, 2018

Last Verified

April 1, 2018

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PSD-toolkit

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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