NCT07785947

Brief Summary

The purpose of the study is to test a program that aims to help staff increase wellness behaviors and test the impact of this program on staff and work outcomes. We will also assess the impact of the program on residents' physical activity and function.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
344

participants targeted

Target at P75+ for not_applicable

Timeline
55mo left

Started Nov 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

August 17, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

August 25, 2026

Completed
2 months until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
4.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2031

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2031

Last Updated

August 25, 2026

Status Verified

August 1, 2026

Enrollment Period

4.5 years

First QC Date

August 17, 2026

Last Update Submit

August 21, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Sedentary, light, moderate and vigorous physical activity

    via an Accelerometer for staff and residents

    -3 months, 0, 3 months, 6 months, 9 months, and 12 months

Secondary Outcomes (15)

  • Sleep duration and quality

    -3 months, 0, 3 months, 6, months, 9 months and 12 months

  • Blood pressure

    -3 months, 0, 3 months, 6 months, 9 months, 12 months

  • Body mass index (BMI)

    -3 months, 0, 3 months, 6 months, 9 months, 12 months

  • Waist circumference

    -3 months, 0, 3 months, 6 months, 9 months, 12 months

  • Visceral fat

    -3 months, 0, 3 months, 6 months, 9 months, 12 months

  • +10 more secondary outcomes

Other Outcomes (2)

  • Quality of interactions schedule (QuIS)

    -3 months, 0, 3 months, 6, months, 9 months, and 12 months

  • Modified Pittsburgh Sleep Quality Index (PSQI)

    -3 months, 0, 3 months, 6, months, 9 months and 12 months

Study Arms (1)

WHHIP with FFC interventions

EXPERIMENTAL

Step 1, Identify a stakeholder team and identify and train an AL champion to work with the interventionist to provide the WHHIP+FFC. Step 2, Environment and policy assessment for PA changes. Step 3, Education and goal setting. Step 4, Mentoring and motivation of staff and residents.

Behavioral: WHHIPBehavioral: FFC

Interventions

WHHIPBEHAVIORAL

Worksite wellness interventions designed to increase physical activity for staff and reduce barriers to physical activity (such as job stress).

WHHIP with FFC interventions
FFCBEHAVIORAL

Interventions designed to increase workers' engagement and encouragement of function focused care with residents

WHHIP with FFC interventions

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • years of age or older
  • employed by the assisted living community in a direct care role for at least 9 months
  • not pregnant
  • speak and understand English

You may not qualify if:

  • do not pass the Evaluation to Sign Consent test
  • do not pass the EASY exercise safety screener
  • years of age or older
  • speak and understand English
  • live in the participating assisting living community at the time of recruitment
  • N/A

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Maryland School of Nursing

Baltimore, Maryland, 21201, United States

Location

MeSH Terms

Conditions

Risk Reduction BehaviorBurnout, ProfessionalMotor Activity

Condition Hierarchy (Ancestors)

BehaviorOccupational StressOccupational DiseasesBurnout, PsychologicalStress, PsychologicalBehavioral Symptoms

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: Incomplete stepped wedge cluster randomized trial design with two pre implementation timepoints (study months -3 and 0) and four timepoints during the intervention (study months 3, 6, 9, and 12).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor

Study Record Dates

First Submitted

August 17, 2026

First Posted

August 25, 2026

Study Start (Estimated)

November 1, 2026

Primary Completion (Estimated)

April 30, 2031

Study Completion (Estimated)

April 30, 2031

Last Updated

August 25, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will share

De-identified raw demographic and outcome data that underlie results in publications

Time Frame
At the end of the study (estimated 2031)
Access Criteria
open access and link will be provided when it is uploaded to the repository

Locations