跳至主要内容
临床试验/NCT03908190
NCT03908190已完成不适用

Pilot Trial of Personalized Support for Progress (PSP) in a VA Women's Wellness Clinic

Syracuse VA Medical Center1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年11月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
28
试验地点
1
主要终点
Assessment Retention Rate

研究概览

简要总结

The purpose of this study is to evaluate the Personalized Support for Progress (PSP) intervention in a Veterans Health Administration (VHA) Women's Wellness Clinic. PSP uses a peer support provider to help women identify their primary concern, develop a personalized plan to help address that concern, and provide practical and emotional support to implement the plan. The primary aim is to evaluate the feasibility, acceptability, and utility of PSP and the research protocol.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

盲法说明

The interviewer evaluating progress towards goals will be blinded to condition.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Veteran status (non-Veterans will not be enrolled in this trial)
  • •Enrollment in the Syracuse VA Medical Center Women's Wellness Clinic
  • •Report high stress within the last month (Perceived Stress Scale [PSS-10] > 18)
  • •Primary Care Provider approval for participation
  • •Ability to communicate in English including reading, writing, hearing, and speaking well enough to complete research and intervention tasks.

排除标准

  • •Any Veteran with "higher" suicide risk on the P4 or Veterans with "lower" suicide risk on the P4 and evaluated by the PI or another clinician to be clinically unstable or at risk
  • •Homicidality (screened via adaptation of the P4 screener and evaluated on the same criteria above)
  • •Homelessness (including literally homeless, imminent risk of homelessness, or fleeing/attempting to flee domestic violence per VA definitions)
  • •Veterans who are enrolled in or have had psychotherapy or changes to psychotropic medications in the last 12 weeks
  • •Veterans with impairment that would not allow them to engage in PSP including active psychosis, cognitive deficits, severe substance use requiring detoxification (documented in CPRS or reported by a PACT member)
  • •Veterans who are not available for outpatient PSP meetings (e.g., in a residential program)
  • •Veterans who have current VA or non-VA peer support engagement (an appointment within the last month and/or additional follow-up scheduled)

研究组 & 干预措施

Treatment As Usual

No Intervention

Participants will receive treatment as usual within the VHA Women's Wellness Clinic including any appropriate treatment or treatments for their medical and psychosocial concerns as determined by their primary care teams.

Treatment As Usual Plus Personalized Support for Progress

Experimental

In addition to treatment as usual, women will receive the Personalized Support for Progress intervention.

干预措施: Personalized Support for Progress (Behavioral)

结局指标

主要结局

Assessment Retention Rate

时间窗: 6 months

This is an assessment of trial feasibility.

Intervention Retention Rate

时间窗: 6 months

This is an assessment of trial feasibility.

Client Satisfaction Questionnaire

时间窗: 6 months

This scale measures satisfaction and ranges from 8-24 with higher scores indicating higher satisfaction.

Goal Attainment Scaling

时间窗: 6 months

This interview assesses progress toward individualized goals on a -2 to 2 scale with higher scores indicating more progress toward goals.

Perceived Stress Scale (PSS-10)

时间窗: 6 months

This scale evaluates perceived stress and ranges from 0-40 with lower scores indicating lower levels of perceived stress.

次要结局

未报告次要终点

研究者

发起方
Syracuse VA Medical Center
申办方类型
Fed
责任方
Principal Investigator
主要研究者

Emily M. Johnson

Psychologist

Syracuse VA Medical Center

研究点 (1)

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