Promoting Positive Care Interactions (PPCI) in Assisted Living (PPCI)

April 23, 2026 updated by: Anju Paudel, PhD, MGS, RN, Penn State University

Optimizing Daily Care Interactions Between Staff and Assisted Living Residents With Alzheimer's Disease and Related Dementias

The overall aim of this study is to pilot test Promoting Positive Care Interactions (PPCI) with the goal of establishing a feasible and culturally responsive approach to optimize care interactions between staff (nursing, activity, housekeeping, and dining service staff) and residents with ADRD in assisted living facilities (ALFs), and further improve select resident, staff, and facility outcomes. PPCI is a non- pharmacological four-step approach consisting of (1) stakeholder engagement in developing facility specific goals; (2) environment and policy assessments; (3) flexible staff education; and (4) ongoing mentorship, motivation, and support (in-person visits and text messages) for staff to optimize care interactions.

Study Overview

Detailed Description

Nearly one million individuals living in 28,900 assisted living facilities (ALFs) in the U.S. participate in daily care interactions, defined as any verbal or nonverbal exchange between staff and residents during physical and social care activities. While there are positive care interactions, poor care interactions also persist with prevalence as high as 25% in long-term care including ALFs. Individuals with Alzheimer's disease and related dementias (ADRD) are especially at risk for poor care interactions due to ineffective staff approaches such as negative touching (e.g., quickly removing clothes to bathe a resident), being overprotective (e.g., restricting activity for safety concerns), and lack of verbal or non-verbal contact during care. Persistent poor care interactions can negatively affect both residents and staff. Thus, there is a need to replace poor care interactions with positive care interactions, now more than ever given the worsening staff retention related to COVID-19 pandemic, and constant need to train new employees.

Positive care interaction refers to care interactions where staff use positive approaches such as honoring resident's abilities and preferences, recognizing resident's responses/non-verbal cues, acknowledging resident's effort, providing role modeling and verbal cues, managing self-responses, and using a calm respectful approach for appropriate delivery of care. It has been long known that use of positive approaches benefits both residents (e.g., less behavioral distress) and staff (e.g., greater competence in care). Yet, poor interactions continue in ALFs due to interlocking barriers associated with residents' ADRD-related communication and other difficulties and behaviors of distress (e.g., agitation), as well as staff's knowledge and training deficits in ADRD care; ALFs have fewer licensing and training mandates for staff. Lack of cultural concordance can also contribute to poor interactions. The ALF staff, often younger (mean age=38.3 yrs.) females (83.8%) with almost half representing racial minorities (47.6%) care for largely non-Hispanic white (81.4%) resident population >=65 years (93.4%). Additionally, there are systemic barriers including limited organizational engagement in implementing and sustaining these approaches, lack of environmental infrastructure (e.g., controlled noise and availability of augmentative devices such as pocket talker) and policies (e.g., consistent assignments) to support positive care interactions, and lack of adequate mentoring and support for staff. It is crucial to address these issues and barriers and train ALF staff on positive care interactions, particularly since prior work has targeted nursing homes and focused on social interactions or verbal communication.

Therefore, this study proposes Promoting Positive Care Interactions (PPCI), a four-step approach, based on Social Ecological Model (SEM) and Social Cognitive Theory (SCT), to optimize daily care interactions between staff and residents with ADRD in ALFs. The four steps include: 1) stakeholder engagement in developing facility specific goals; (2) environment and policy assessments; (3) flexible staff education; and (4) ongoing mentorship, motivation, and support (in-person visits and text messages) for staff to optimize care interactions. These four steps are based on prior work implementing function & behavior focused intervention studies but have never been used in a care interaction-focused intervention nor been tested for cultural responsiveness. This study will follow a cluster randomized trial in a sample of 60 residents and 60 staff in four ALFs in central PA (approx. 15 residents, 15 staff/ALF) who agree and consent to participate in this study. The treatment group will receive all four steps of PPCI while the control arm will receive education only.

Study Type

Interventional

Enrollment (Actual)

130

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Pennsylvania
      • University Park, Pennsylvania, United States, 16802
        • The Pennsylvania State University

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

65 years and older (Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

Assisted Living Facility (ALF) will be included in the study if they:

  1. have at least 20 or more beds
  2. are able to identify a facility champion, and
  3. express a willingness to actively partner in an initiative to change practice at their institution

Staff will be included in the study if they:

  1. are able to communicate in English, and
  2. work at least 16 hours a week at the facility at the time of recruitment in nursing, activities, housekeeping, or dining service roles

Residents will be included in the study if they:

  1. are 65 years old or greater
  2. are living at the facility at the time of recruitment, and
  3. have a diagnosis of ADRD and Saint Louis University Mental Status Exam (SLUMS) score of 20 or less (high school education)/ 19 or less (less than high school education) suggesting ADRD

Exclusion Criteria:

Assisted Living Facility (ALF) will be excluded from the study if they:

  1. have less than 20 beds
  2. are unable to identify a facility champion, and
  3. do not express a willingness to actively partner in an initiative to change practice at their institution

Staff will be included in the study if they:

  1. are unable to communicate in English, and
  2. work less than16 hours a week at the facility at the time of recruitment in nursing, activities, housekeeping, or dining service roles

Residents will be included in the study if they:

  1. are less than 65 years old
  2. are not living at the facility at the time of recruitment, and
  3. do not have a diagnosis of ADRD and Saint Louis University Mental Status Exam (SLUMS) score of 20 or less (high school education)/ 19 or less (less than high school education) suggesting ADRD

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

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: PPCI Arm
The ALF/PCH assigned as treatments will receive the four steps of PPCI including, stakeholder engagement and facility goal development, environment and policy assessment, staff education, and ongoing mentorship/motivation and support over a period of six-months by a research nurse facilitator (RNF), a registered nurse (RN) with prior experience in long-term care. The RNF will work with an identified internal/facility champion monthly to implement the four steps of PPCI.

The PPCI consists of four steps: (1) stakeholder engagement in developing facility specific goals; (2) environment and policy assessments; (3) flexible staff education; and (4) ongoing mentorship, motivation, and support (in-person visits and text messages) for staff to optimize care interactions.

A research nurse facilitator (RNF), a registered nurse (RN) with prior experience in long-term care will work with an identified internal champion monthly to implement the four steps of PPCI. The PPCI intervention comprehensively focuses on intrapersonal, interpersonal, organizational, and environmental/policy factors to bring together evidence and key stakeholders to optimize daily care interactions in assisted living.

Active Comparator: PPCI-Staff Education Only Arm
The ALF/PCH assigned as controls will receive PPCI-staff education only (EO). The EO will include a 30-45 min in-service session and monthly f/u visits for booster education. The education content and process will be the same as outlined in Step 3 of the PPCI for treatment sites.
The EO will include a 30-45 min in-service session and monthly f/u visits for booster education. The education content and process will be the same as outlined in Step 3 of the PPCI for treatment sites.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The degree to which the intervention can be implemented as intended assessed by Feasibility of Intervention Measure (FIM) Questionnaire
Time Frame: six-months post intervention
4 items answered on a 5-point ordinal scale ranging from 'completely disagree' to 'completely agree'; range = 4 to 20 and higher scores are better
six-months post intervention
The degree to which the intervention is acceptable assessed by Acceptability of Intervention Measure (AIM) Questionnaire
Time Frame: six-months post intervention
4 items answered on a 5-point ordinal scale ranging from 'completely disagree' to 'completely agree'; range = 4 to 20 and higher scores are better
six-months post intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Well-being assessed by Quality of Life in Late-stage Dementia (QUALID) Scale
Time Frame: baseline and 6 months
11 items on a 5-point scale, range = 11 to 55 and higher scores are better
baseline and 6 months
Level of agitation assessed by Cohen-Mansfield Agitation Inventory (CMAI-short form)
Time Frame: baseline and 6 months
14 items answered on a 5-point scale, range = 14 to 70 and lower scores are better
baseline and 6 months
Frequency and intensity of resistive behaviors assessed by Resistiveness to Care (RTC) Scale
Time Frame: baseline and 6 months
13 items answered on a 3-point scale for intensity and a number provided for frequency, range = 13 to 39 for intensity and lower scores are better
baseline and 6 months
Knowledge of person-centered behavioral approaches for managing behavioral symptoms of distress assessed by Knowledge of Person-Centered Behavioral Approaches for BPSD
Time Frame: baseline and 6 months
10 items with four responses (1 correct, 3 distracters), range = 0 to 10 and higher scores are better
baseline and 6 months
Perceived competence in dementia care assessed by Sense of Competence in Dementia Care Staff (SCIDS)
Time Frame: baseline and 6 months
17 items on a 4-point scale, range = 17 to 68 and higher scores are better
baseline and 6 months
Level of stress assessed by Health Professions Stress Inventory (HPSI)
Time Frame: baseline and 6 months
12 items on a 5-point scale, range = 0 to 48 and lower scores are better
baseline and 6 months
Staff-resident relationship quality assessed by Positive Affect Index (PAI)
Time Frame: baseline and 6 months
5 items on a 6-point scale, range = 5 to 30 and higher scores are better
baseline and 6 months
Staff-resident care interactions assessed by Quality of Care Interactions Schedule (QuIS)
Time Frame: baseline and 6 months
5 items answered on a 3-point scale, range = 0 to 7 and higher scores are better
baseline and 6 months
Provision of facility policies pertaining to promoting positive care interactions (PPCI) assessed by Assessment of Policies for PPCI
Time Frame: baseline and 6 months
24 items answered as yes (1) or no (0), range = 0 to 24 and higher scores are better
baseline and 6 months
Provision of facility environment pertaining to promoting positive care interactions (PPCI) assessed by Assessment of Environment for PPCI
Time Frame: baseline and 6 months
23 items answered as yes (1) or no (0), range = 0 to 23 and higher scores are better
baseline and 6 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cultural responsiveness assessed by a questionaire based on the ecological model (EM) domains: language, persons, metaphors, goals, content, concepts, methods, & context of PPCI
Time Frame: six-months post intervention
12 interview questions
six-months post intervention

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Anju Paudel, Assistant Professor, Penn State University

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)

March 3, 2025

Primary Completion (Actual)

December 8, 2025

Study Completion (Actual)

March 11, 2026

Study Registration Dates

First Submitted

October 31, 2022

First Submitted That Met QC Criteria

November 8, 2022

First Posted (Actual)

November 16, 2022

Study Record Updates

Last Update Posted (Actual)

April 27, 2026

Last Update Submitted That Met QC Criteria

April 23, 2026

Last Verified

August 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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