Testing Effectiveness of a Peer-Led Intervention to Enhance Community Integration
Status: | Completed |
---|---|
Conditions: | Psychiatric, Psychiatric |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/28/2019 |
Start Date: | March 5, 2015 |
End Date: | February 15, 2019 |
We are conducting a randomized clinical trial (RCT) comparing the 10-week peer-led Photovoice
program to services as usual (SAU) at a large publicly funded community mental health agency
in Massachusetts. The control SAU condition will be enhanced with a 60-minute peer-led group
educational session about understanding and coping with prejudice and discrimination. The
10-session, peer-led Photovoice program, designed to empower individuals with serious mental
illness (SMI) to confront public prejudice and discrimination and reduce personal stigma
(self-stigma and perceived stigma), was developed and pilot tested at our Center, with
primary contributions from staff with a lived experience of mental illness. Development of
the Photovoice program was guided by an adaptation of the stress-coping model, informed by
recent research and conceptualizations of the effects of stigma on people with SMI. The
stress-coping model explicates the mechanisms by which public stigma about mental illness can
lead to personal stigma, which in turn has a negative impact on the person's mental health
and psychosocial functioning. This model also identifies critical factors that contribute to
personal stigma or protect against it, as well as more vs. less adaptive coping responses,
that are the primary focus of the Photovoice program.
program to services as usual (SAU) at a large publicly funded community mental health agency
in Massachusetts. The control SAU condition will be enhanced with a 60-minute peer-led group
educational session about understanding and coping with prejudice and discrimination. The
10-session, peer-led Photovoice program, designed to empower individuals with serious mental
illness (SMI) to confront public prejudice and discrimination and reduce personal stigma
(self-stigma and perceived stigma), was developed and pilot tested at our Center, with
primary contributions from staff with a lived experience of mental illness. Development of
the Photovoice program was guided by an adaptation of the stress-coping model, informed by
recent research and conceptualizations of the effects of stigma on people with SMI. The
stress-coping model explicates the mechanisms by which public stigma about mental illness can
lead to personal stigma, which in turn has a negative impact on the person's mental health
and psychosocial functioning. This model also identifies critical factors that contribute to
personal stigma or protect against it, as well as more vs. less adaptive coping responses,
that are the primary focus of the Photovoice program.
We are conducting a RCT comparing the 10-week peer-led Photovoice program to services as
usual (SAU) enhanced with a 60-minute peer-led group discussion session. The RCT will be at a
large publicly funded community mental health agency in Massachusetts. A total of 192
participants or 96 participants per group will be recruited over a period of 36 months across
the three clubhouses of the agency where the intervention will take place. We plan to have
randomization cohorts of 16 individuals per delivery of the Photovoice program at each of the
three clubhouses. Given the projected sample size of 192 participants, we will have 12
randomization cohorts - 4 at each clubhouse implemented at 6-month intervals. Participants
will be randomized to either the Photovoice program (plus usual services) or the enhanced
SAU. Participants will be assessed by a blinded rater at baseline, post-treatment, 3-month
and 6-month follow-ups on a range of primary and secondary outcomes related to personal
stigma, coping, and functioning. Primary analyses will test the hypotheses that the
Photovoice program will lead to significantly greater reductions in self-stigma and perceived
stigma, greater improvements in proactive coping with psychiatric prejudice and
discrimination, and greater improvements in community functioning and integration than the
enhanced SAU. Secondary analyses will evaluate whether the Photovoice program leads to
greater gains than SAU in psychological adjustment, including wellbeing, personal growth and
recovery. Individuals randomized to the enhanced SAU will be able to join the 10-week
Photovoice program once they complete their 6-month follow up for the study.
usual (SAU) enhanced with a 60-minute peer-led group discussion session. The RCT will be at a
large publicly funded community mental health agency in Massachusetts. A total of 192
participants or 96 participants per group will be recruited over a period of 36 months across
the three clubhouses of the agency where the intervention will take place. We plan to have
randomization cohorts of 16 individuals per delivery of the Photovoice program at each of the
three clubhouses. Given the projected sample size of 192 participants, we will have 12
randomization cohorts - 4 at each clubhouse implemented at 6-month intervals. Participants
will be randomized to either the Photovoice program (plus usual services) or the enhanced
SAU. Participants will be assessed by a blinded rater at baseline, post-treatment, 3-month
and 6-month follow-ups on a range of primary and secondary outcomes related to personal
stigma, coping, and functioning. Primary analyses will test the hypotheses that the
Photovoice program will lead to significantly greater reductions in self-stigma and perceived
stigma, greater improvements in proactive coping with psychiatric prejudice and
discrimination, and greater improvements in community functioning and integration than the
enhanced SAU. Secondary analyses will evaluate whether the Photovoice program leads to
greater gains than SAU in psychological adjustment, including wellbeing, personal growth and
recovery. Individuals randomized to the enhanced SAU will be able to join the 10-week
Photovoice program once they complete their 6-month follow up for the study.
Inclusion Criteria:
- Age 18years and older
- Diagnosis of serious mental illness
- Receiving services at agency where study is taking place
- Willing and able to give written consent
- Conversant in English
Exclusion Criteria:
- Prior exposure to Photovoice
- Cognitive disability
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