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Partnership in Implementation Science for Geriatric Mental Health (PRISM)

Not Applicable
Conditions
Behavioral and Psychological Symptoms of Dementia (BPSD)
Interventions
Behavioral: Physical Exercise Intervention
Registration Number
NCT03264378
Lead Sponsor
Brigham and Women's Hospital
Brief Summary

The Partnership in Implementation Science for Geriatric Mental Health (PRISM) project proposes an evidence-based physical exercise intervention for older adults who exhibit behavioral and psychological symptoms of dementia (BPSD). The proposed evaluation study will conduct a randomized controlled trial with a Hybrid Type 3 design to compare the intervention arm that implements the culturally-adapted GTO model (GTO-ThAI) to deliver implementation support, with a control arm, which receives usual top-down administrative instruction for implementing a policy initiative.

Detailed Description

The overall goal of this project is to establish a hub to integrate implementation research for scaling up sustainable, evidence-based mental health interventions with research capacity-building activities for East Asia. Specific scale-up study aims include: Aim 1: Assessing readiness for implementing the evidence-based physical exercise intervention for improving mental health of older adults in participating provinces of Thailand; Aim 2: Developing the GTO-ThAI implementation support model through a pre-implementation case study and formative evaluation; and Aim 3: Evaluation of implementation strategies and clinical outcomes through a hybrid Type 3 randomized trial to test an evidence-based implementation support strategy (i.e., the GTO-ThAI model) that emphasizes a systematic process to address implementation barriers to the delivery of the evidence-based physical exercise intervention (PEI), compared with the existing standard administrative procedures for delivering the same PEI.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
350
Inclusion Criteria
  • (a) adults who are aged 55 and older,
  • (b) screen positive for dementia,
  • (c) screen positive for BPSD, and
  • (d) having a caregiver who is willing to participate in the study.
Exclusion Criteria
  • (a) caregivers who are cognitively not intact, and/or
  • (b) not willing to participate in the intervention.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PEI-GTO-ThAIPhysical Exercise InterventionPhysical exercise intervention (PEI) supported by the GTO-ThAI Implementation Model
PEI-StandardPhysical Exercise InterventionPhysical exercise intervention (PEI) supported by the standard governmental administrative procedures
Primary Outcome Measures
NameTimeMethod
Implementation outcome scoreUp to 12 months

Adapted from the Quality Implementation Tool (Meyer et al., 2012), using a total score based on average of ratings, by site implementation team leaders, on a 7-point Likert scale over 48 items across eight dimensions of implementation (e.g. adoption, fidelity, dosage, program reach, differentiation, quality of implementation, implementation cost, sustainability).

Secondary Outcome Measures
NameTimeMethod
Behavioral and psychological symptoms of dementia (BPSD)Up to 12 months

BPSD will be assessed by the Neuropsychiatric Inventory (NPI), using the total score obtained by summing all the individual domain total scores; each domain score is the product of the frequency score multiplied by the severity score for that behavioral domain.

Trial Locations

Locations (1)

Ministry of Public Health

🇹🇭

Bangkok, Thailand

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