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Training and Coaching to Promote High Performance in Veteran Affairs (VA) Nursing Home Care

Training and Coaching to Promote High Performance in VA Nursing Home Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00875706
Enrollment
45
Registered
2009-04-03
Start date
2009-10-31
Completion date
2011-03-31
Last updated
2015-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Keywords

Nursing Homes, Implementation of innovative programs, Nursing staff, Nurses' aides, Educational models

Brief summary

This study aimed to explore the feasibility of an educational intervention to strengthen workplace learning systems in four VA Community Living Centers (CLCs).

Detailed description

Background: The study explored the feasibility of an educational intervention to strengthen workplace-learning systems in four VA Community Living Centers (CLCs). Objectives: Specific aims were to 1) conduct a feasibility study to assess whether the educational intervention is practical to implement as designed and 2) conduct a pilot study to validate the methodology proposed for assessing outcomes of this educational intervention. Methods: A multi-level intervention targeting the translation of workplace learning into practice was implemented. The Direct Care Worker (DCW) intervention targeted both clinical knowledge and effective communication. The Coaching Supervision training addressed management and supervision practices for nurses, combined with effective communication. Four CLCs received both interventions, administered by the Paraprofessional Health Institute (PHI), using a train-the-trainer approach over the course of four 3-day sessions. Quantitative and qualitative data were collected to assess factors influencing effectiveness of implementation and to understand the impact of the trainings on participants. Status: The study has been completed with educational interventions implemented and qualitative and quantitative data collected.

Interventions

BEHAVIORALEducational Intervention

The intervention consists of two (2) different types of training, both to be delivered through a train-the-trainer approach. The first of these is coaching-supervision training for nurse managers and other supervisory personnel in the CLC units. The second component is a one-day training for DCWs on communication and managing problem behaviors associated with dementia. These two trainings build on validated training models that have been developed by PHINational, but will be adapted and customized to include VA-developed clinical content on the management of problem behaviors associated with dementia.

Sponsors

US Department of Veterans Affairs
Lead SponsorFED

Study design

Allocation
NON_RANDOMIZED
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* VA Employees: psychologists, nurse-managers and front-line nursing care staff assigned to CLCs will be included

Exclusion criteria

* Those not working in the CLC, * Those working in the CLC but not involved in the training intervention that is the focus of the study (e.g. Environment Management Service personnel, dietary personnel)

Design outcomes

Primary

MeasureTime frameDescription
Completion of Training InterventionThis outcome was assessed at the end of the 1 year pilot study.This outcome measures the number of participants that fully completed the training intervention.
Facility Implementation of TrainingsThis outcome was assessed at the end of the 1 year pilot study.This measure assesses the number of participating facilities (4) that implemented trainings in their own facilities upon completion of our educational training intervention.
Number of Participants in Pilot SurveysThis outcome was assessed at the end of the 1 year pilot study.This outcome measures the number of participants that completed the survey during the pilot in order to assess the feasibility of conducting a larger study.
Number of Participants in Pilot InterviewsThis outcome was assessed at the end of the 1 year pilot study.This outcome measures the number of participants that participated in interviews that were conducted during the pilot in order to assess the feasibility of conducting a larger study.

Countries

United States

Participant flow

Participants by arm

ArmCount
Training Feasibility
4 sites (8 individuals) received the training intervention to determine the feasibility of the train-the trainer approach. The educational intervention is included in this arm.
8
Data Collection - Survey
Survey data collection tools were piloted to assess feasibility of survey administration and development of the survey for future studies. These tools were piloted in sites where the educational intervention was administered.
24
Data Collection - Interview
Interview data collection tools were piloted to assess feasibility of interview administration and development of the interview protocol for future studies. These tools were piloted in sites where the educational intervention was administered.
13
Total45

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyWithdrawal by Subject100

Baseline characteristics

CharacteristicData Collection - InterviewTotalTraining FeasibilityData Collection - Survey
Age, Categorical
<=18 years
NA ParticipantsNA ParticipantsNA ParticipantsNA Participants
Age, Categorical
>=65 years
NA ParticipantsNA ParticipantsNA ParticipantsNA Participants
Age, Categorical
Between 18 and 65 years
NA ParticipantsNA ParticipantsNA ParticipantsNA Participants
Race/Ethnicity, Customized
American Indian/Alaskan Native
NA participantsNA participantsNA participants0 participants
Race/Ethnicity, Customized
Asian
NA participantsNA participantsNA participants0 participants
Race/Ethnicity, Customized
Black
NA participantsNA participantsNA participants5 participants
Race/Ethnicity, Customized
Native Hawaiian/Other Pacific Islander
NA participantsNA participantsNA participants0 participants
Race/Ethnicity, Customized
Unknown
NA participantsNA participantsNA participants2 participants
Race/Ethnicity, Customized
White
NA participantsNA participantsNA participants17 participants
Sex/Gender, Customized
Female
NA participantsNA participantsNA participants19 participants
Sex/Gender, Customized
Male
NA participantsNA participantsNA participants4 participants
Sex/Gender, Customized
Unknown
NA participantsNA participantsNA participants1 participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
— / —— / —— / —
other
Total, other adverse events
0 / 00 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 00 / 0

Outcome results

Primary

Completion of Training Intervention

This outcome measures the number of participants that fully completed the training intervention.

Time frame: This outcome was assessed at the end of the 1 year pilot study.

Population: The analysis population includes only participants who started the Train-the-Trainer intervention and therefore only participants in the Training Feasibility Arm/Group were analyzed for this outcome.

ArmMeasureValue (NUMBER)
Training FeasibilityCompletion of Training Intervention7 participants
Primary

Facility Implementation of Trainings

This measure assesses the number of participating facilities (4) that implemented trainings in their own facilities upon completion of our educational training intervention.

Time frame: This outcome was assessed at the end of the 1 year pilot study.

Population: This unit of measure for this outcome measure is at the facility level. There were 4 facilities (8 trainees) in total that began the training intervention.

ArmMeasureGroupValue (NUMBER)
Training FeasibilityFacility Implementation of TrainingsCoaching and Supervision Training3 Facility
Training FeasibilityFacility Implementation of TrainingsDirect Care Worker Training2 Facility
Primary

Number of Participants in Pilot Interviews

This outcome measures the number of participants that participated in interviews that were conducted during the pilot in order to assess the feasibility of conducting a larger study.

Time frame: This outcome was assessed at the end of the 1 year pilot study.

Population: Only participants in the Data Collection - Interview group were analyzed for this outcome. The population included trainees and direct care workers.

ArmMeasureValue (NUMBER)
Data Collection - InterviewNumber of Participants in Pilot Interviews13 participants
Primary

Number of Participants in Pilot Surveys

This outcome measures the number of participants that completed the survey during the pilot in order to assess the feasibility of conducting a larger study.

Time frame: This outcome was assessed at the end of the 1 year pilot study.

Population: Only participants in the Data Collection - Survey group were analyzed for this outcome. The population included trainees and direct care workers.

ArmMeasureValue (NUMBER)
Data Collection - SurveyNumber of Participants in Pilot Surveys24 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026