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Minnesota Inclusive LTSS for LGBTQ Seniors (MILLS)

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Enrolling

Conditions

Alzheimer Disease
Dementia

Treatments

Other: Training to Serve (TTS) in person training
Other: Training to Serve online training (eTTS)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05530590
5R01AG075734 (U.S. NIH Grant/Contract)
STUDY00014177

Details and patient eligibility

About

This study is designed to help improve the care of sexual and gender minority (SGM) with Alzheimer's Disease and Alzheimer's Disease Related Dementia (AD/ADRD) in long-term services and supports (LTSS) by training the state's LTSS workforce in SGM culturally responsive care. The randomized controlled trial will rigorously test the effects of an in person versus an online training program on improving SGM culturally responsive care with a waitlist control.

Full description

The study involves conducting a 3-arm, stratified (management/staff), group (agency) randomized controlled trial (RCT) of the in-person vs. online intervention vs. waitlist control on organizational factors (i.e., environment and policy) and on staff knowledge, attitudes, and skills.

Enrollment

760 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • licensure in Minnesota to provide nursing and/or as a housing with services establishment
  • Willingness to undertake a policy and environment review at baseline and 6 months later
  • having at least 5 managers/ supervisors and 5 staff.

Exclusion criteria

  • Participants who cannot speak and read English

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

760 participants in 3 patient groups

Training to Serve (TTS) in person training
Experimental group
Description:
Participants are provided access to the pretest one week before the training. On the day of training, when the trainers arrive, participants have a final opportunity to complete the baseline survey before the intervention. Tablets will be available to complete pre- and post- surveys. The training for management takes 3-4 hours, and for staff, one hour. For consistency and feasibility, both trainings are conducted by the same trainers at the same visit. Immediately after the intervention, participants complete the post-intervention seminar evaluation assessing knowledge and attitudes/comfort in serving SGM clients.
Treatment:
Other: Training to Serve (TTS) in person training
Training to Serve online training (eTTS)
Experimental group
Description:
Participants are provided a unique identifier to access the online website. The opening page welcomes them to the study, then directs them to the chunked consent materials and baseline survey. As soon as they have completed this, they receive access to the intervention, which for management is expected to take 1-2 hours and for staff, 30-45 minutes (i.e., the online equivalent of 3-4 and 1 hour, respectively). After completion of the required modules, participants receive access to the optional modules as well as the posttest survey to evaluate the training. Once the post-test is complete, they are thanked for their involvement and informed they will receive an e-mail to access a follow-up survey in six months' time.
Treatment:
Other: Training to Serve online training (eTTS)
Waitlist control
No Intervention group
Description:
Participants complete the baseline survey, then they receive a note thanking them for completing all activities and informing them the intervention will be available in 6 months' time.

Trial contacts and locations

1

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Central trial contact

Simon Rosser, PhD,MPH

Data sourced from clinicaltrials.gov

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