Skip to content

Texting for Relapse Prevention

Texting for Relapse Prevention Among People Diagnosed With Schizophrenia or SAD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02819349
Acronym
T4RP
Enrollment
40
Registered
2016-06-30
Start date
2018-03-12
Completion date
2019-04-09
Last updated
2020-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizoaffective Disorder, Schizophrenia

Keywords

Relapse Prevention, People with Schizophrenia, Text-Messaging, Assertive Community Treatment (ACT)

Brief summary

The purpose of this study is to examine whether Texting for Relapse Prevention (T4RP), a text messaging-based early warming for relapse prevention in people who have schizophrenia/SAD, is associated with fewer relapse symptoms compared to a treatment-as-usual control group.

Detailed description

Schizophrenia is among the 20 most debilitating illnesses worldwide, responsible for 1% of the global burden of disease. Schizoaffective disorder (SAD) affects an additional 0.2% to 1.1% of adults. As many as four out of five people who have schizophrenia or SAD relapse within 5 years of recovery from their initial episode. Interventions aimed at early intervention to prevent relapse would impact public health. The Texting for Relapse Prevention (T4RP) is an innovative service delivery program delivered via text messaging designed for people who have schizophrenia/SAD. The intervention will be tested in a randomized controlled trial against a treatment-as-usual control group which, for most, involved meeting with their therapist every 2 to 4 weeks and meeting with their psychiatrist at least once every 90 days or more frequently as clinically indicated. A total of 40 people with schizophrenia and 5-15 provider participants (depending on the patient distribution across the providers) in the pilot RTC. The study is being conducted by researchers at the Center for Innovative Public Health Research and Johns Hopkins Community Psychiatry Program (JHCPP). The investigators posit that T4RP will reduce psychiatric morbidity and institutionalization rates and promote recovery by facilitating improved patient-provider communication, promoting medication adherence, helping people self-monitor their early warning signs, and promoting self-management of symptoms. If T4RP is effective, this cost-effective and easily scalable intervention will make a significant public health impact and reduction in relapse-related costs for people with schizophrenia/SAD.

Interventions

BEHAVIORALTexting for Relapse Prevention (T4RP)

T4RP is a relapse prevention mHealth program text messaging to people who have schizophrenia/SAD. Content is guided by components of the Assertive Community Treatment (ACT) and focuses on facilitating improved patient-provider communication, promoting medication adherence, helping people self-monitor their early warning signs, and promoting self-management of symptoms.

Sponsors

Johns Hopkins University
CollaboratorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH
Center for Innovative Public Health Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* be English-speaking; * have a chart diagnosis of schizophrenia or SAD * be able to provide consent (i.e., pass the Capacity to Consent screen) * own a cell phone and report using the text messaging function * be currently at their personal baseline with regard to symptoms and functioning as assessed by their provider (i.e., not in relapse and compliant with treatment) * be actively under the care of a mental health provider enrolled in the program * agree to continue attending the clinic for the duration of the study * plan to keep the same cell phone number for the duration of the study * have at least one of their providers consent to take part in the study

Exclusion criteria

* have at least one of their providers consent to take part in the study

Design outcomes

Primary

MeasureTime frameDescription
Recovery Assessment Scale6-months post-study enrollmentIt is a 41-item self-report scale with 5 subscales that measure an individual's experience of recovery
Montgomery-Asberg Depression Scale (MADRS)6-months post-study enrollmentIt is a clinician-administered 10-item scale developed to measure changes in depressive symptom during treatment.
Young Mania Rating Scale (YMRS)6-months post-study enrollmentIt is is an 11-item clinician administered scale that assesses the presence and severity of manic symptoms.
Institutionalization6-months post-study enrollmentThe number of hospitalizations or ER crisis visits during the study period
The Positive and Negative Syndrome Scale (PANSS)6-months post-study enrollmentIt has three subscales that measure: positive symptoms of schizophrenia, negative symptoms of schizophrenia, and general psychopathology.

Secondary

MeasureTime frameDescription
Boston University Empowerment Scale6-months post-interventionIt is a 28-item self-report scale that measures empowerment among those using mental health services.
Brief Cognitive Assessment6-months post-interventionIt is a clinician administered test that consists of 3 standard tests: Verbal Fluency, Hopkins Verbal Learning Test and Trails A and B and has been shown to be related to measures of functional outcome in patients with schizophrenia.
Brief Adherence Rating Scale6-months post-interventionIt is a clinician-administered, 4-item scale that has three questions and an overall visual analog scale. It was designed for use in community settings with individuals who have schizophrenia or schizoaffective disorder and has been validated against electronically-monitored adherence.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026