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临床试验/NCT04545593
NCT04545593
已完成
不适用

Building Community Capacity for Disability Prevention for Minority Elders - Renewal

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 427 人2021年2月11日

概览

阶段
不适用
干预措施
Positive Minds Strong Bodies Enhanced
疾病 / 适应症
Depression
发起方
Massachusetts General Hospital
入组人数
427
试验地点
2
主要终点
Hopkins Symptom Checklist-25 (change)
状态
已完成
最后更新
11天前

概览

简要总结

This study aims to address treatment and service disparities and prevent disability among racial/ethnic and linguistic minority elders. It tests the effectiveness and implementation readiness of the Positive Minds-Strong Bodies Enhanced intervention (PMSB-E), a combined mental and physical health intervention designed to be implemented in low-resource community settings. This renewal grant project includes a streamlined intervention with new components designed to improve and maintain participant outcomes.

详细描述

The Positive Minds-Strong Bodies Enhanced intervention addresses the dual challenges of mental health and physical disability among minority elders. The core Positive Minds intervention includes 10 sessions offered by Community Health Workers over a maximum of 6 months, designed to identify and correct negative distortions or cognitions, promote behavioral activation and encourage supportive relationships. Strong Bodies is a 36-session physical intervention consisting of a series of exercises conducted while wearing a weighted vest in a group setting over 6 months; both interventions include a group maintenance component to maintain gains. The investigators will evaluate the acceptability, effectiveness and twelve-month sustainability of the Enhanced Positive Minds-Strong Bodies intervention (E-PMSB) offered by Community Health Workers (CHWs) and Exercise Trainers in community-based organizations (CBOs) and community clinics. The intervention is offered in English, Spanish, Mandarin or Cantonese.

注册库
clinicaltrials.gov
开始日期
2021年2月11日
结束日期
2024年10月31日
最后更新
11天前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Margarita Alegria, PhD

Chief, Disparities Research Unit

Massachusetts General Hospital

入排标准

入选标准

  • Latino, Asian, Black, or non-Latino White adults 60+ years of age
  • With mild, moderate or severe depressive or anxiety symptoms.
  • Participants receiving medications for mental health will have this recorded and used as a covariate.
  • Community-dwelling participants who have some mobility limitations but are not home-bound.

排除标准

  • Any specialty mental health care (therapy sessions with psychiatrist, psychologist or social worker) in the past 3 months or scheduled in the coming month.
  • Evidence that patient lacks capacity to consent or is cognitively impaired
  • Current suicidal risk (score of 4 or 5 on Paykel suicide questionnaire), whereby participant will be connected to an emergency services or specialty provider per the study emergency protocol.
  • Physically instability, acute or exacerbation of a chronic disease, or a neuro-musculoskeletal impairment
  • Severe substance abuse
  • Self-reported psychosis or schizophrenia
  • Inability to commit to 2 sessions per week

研究组 & 干预措施

Positive Minds Strong Bodies Enhanced

The Positive Minds Strong Bodies Enhanced intervention (PMSB-E) consists of 10 sessions focused on mental health (PM) and 36 sessions focused on physical health (SB), along with a group maintenance component.

干预措施: Positive Minds Strong Bodies Enhanced

Enhanced Usual Care

The Enhanced Usual Care condition includes written materials on depression and anxiety and 4 calls to participants over the course of 6 months to assess symptoms and safety.

干预措施: Enhanced Usual Care

结局指标

主要结局

Hopkins Symptom Checklist-25 (change)

时间窗: Baseline and 3, 6, and 12 months after baseline

Widely used measure of depression and anxiety in clinical monitoring and outcome assessment.

Acceptability

时间窗: 6 months at end of treatment

\>/= 70% of participants attending \>/= 50% of their intervention sessions, reporting satisfaction with treatment.

Late-Life Function and Disability Instrument (LLFDI) - functional component (change)

时间窗: Baseline and 3, 6, and 12 months after baseline

Self-report instrument designed to measure both functional capacity and components of disability.

Short Physical Performance Battery (change)

时间窗: Baseline and 3, 6, and 12 months after baseline

Assessment of standing balance, timed 4-m walk, and timed test of five chair-rise repetitions, to assess functional limitations. A virtual option will be used while in person assessment is not possible due to COVID-19.

Acceptability

时间窗: 12 months after baseline

\>/= 70% of participants attending \>/= 50% of their intervention sessions, reporting satisfaction with treatment. This outcome was measured among intervention participants only (Positive Minds Strong Bodies Enhanced) using four indicator variables for attending 5+ (out of 10) PM intervention sessions, 18+ (out of 36) SB intervention sessions, being very satisfied with the care received by intervention provider, and being very satisfied with the program.

Depression and Anxiety Symptoms as Assessed by Hopkins Symptom Checklist-25

时间窗: 3, 6, and 12 months after baseline

The Hopkins Symptom Checklist-25 (HSCL-25) assessed past 2-week self-reported symptoms of depression and anxiety. The HSCL-25 includes 25 items, each rated from 1 (not at all) to 4 (extremely). Total raw scores are calculated by averaging all items (range 1 to 4, with higher scores indicating more severe symptoms). Model-estimated marginal means for each treatment group at each follow-up timepoint were obtained using linear mixed-effects models with repeated measures of HSCL-25 scores across follow-up assessments, adjusting for baseline HSCL-25 scores.

Physical Functioning as Assessed by Short Physical Performance Battery

时间窗: 3, 6, and 12 months after baseline

The Short Physical Performance Battery (SPPB) objectively assessed physical functioning through balance, gait, and chair-rise timed tests. A summary performance score is calculated by summing categorical rankings on the three tests (range 0 to 12, with higher scores indicating better performance). Model-estimated marginal means for each treatment group at each follow-up timepoint were obtained using linear mixed-effects models with repeated measures of SPPB scores across follow-up assessments, adjusting for baseline SPPB scores.

Physical Functioning as Assessed by the Function Component of the Late-Life Functioning and Disability Instrument

时间窗: 3, 6, and 12 months after baseline

The Function Component of the Late-Life Functioning and Disability Instrument (LLFDI) assessed self-reported physical functioning, with 32 items assessing difficulty (1 'cannot do' to 5 'none') to perform discrete actions or activities without the help of someone else or using assistive devices. Total scores are calculated by summing all items (range 32 to 160, with higher scores indicating fewer difficulties). Model-estimated marginal means for each treatment group at each follow-up timepoint were obtained using linear mixed-effects models with repeated measures of LLFDI scores across follow-up assessments, adjusting for baseline LLFDI scores.

次要结局

  • Disability as Assessed by World Health Organization Disability Assessment Schedule 2.0(3, 6, and 12 months after baseline)

研究点 (2)

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