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ReliefLink: A Preventative Mobile Toolkit for Follow-Up Care of Psychiatric Patients

ReliefLink: A Preventative Mobile Toolkit for Follow-Up Care of Psychiatric Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02691221
Enrollment
13
Registered
2016-02-25
Start date
2016-04-30
Completion date
2017-10-31
Last updated
2017-12-15

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

Conditions

Suicide, Suicidal Ideation

Keywords

Suicidal behavior, Mobile Application, Mobile Health Tool

Brief summary

The purpose of this study is to increase use and availability, as well as assess the feasibility of the ReliefLink (RL) application for use in conjunction with standard care to promote psychological health and prevent suicidal behavior.

Detailed description

The aims of this study of ReliefLink application are to determine the utility of ReliefLink self-reports of suicidal ideation, negative emotions, loneliness, subjective well-being, flourishing, mental toughness, positive emotions, learned optimism, resilience, and post-traumatic growth. Additional aims are to evaluate the impact of ReliefLink on perceived access to/usage of care and resources and to explore participant acceptance of ReliefLink as a technological support for standard treatment through human systems engineering of treatment plan adherence and user interview.

Interventions

BEHAVIORALRelief Link Application Daily Tasks

Participants will complete daily mood tracking and completion of a minimum of one stress management activity per day. Relaxation exercises to choose from on the current version of RL are audio files (i.e., no visuals), and consist of: Guided Meditation, Energizing Breath, Guided Visualization for Relaxation, Progressive Relaxation, Mindfulness Meditation Body Scan, and Mindfulness of Breathing.

Sponsors

Georgia Institute of Technology
CollaboratorOTHER
Emory University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Enrolled as patients seeking behavioral health treatment through the Grady Health System * Speak English * Sought inpatient and/or outpatient treatment with Grady Health System following a suicide attempt or ideation. * Has personal access to a functioning iPhone and service plan.

Exclusion criteria

* Has significant cognitive impairments. * Is actively psychotic or has an imminently life-threatening medical/psychiatric condition per provider evaluation.

Design outcomes

Primary

MeasureTime frameDescription
Change in scores on 6 item Columbia Suicide Severity Rating Scale Screener (C-SSRS)Baseline, 6 MonthsA comprehensive, semi-structured interview measure that uniquely measures the full spectrum of suicidality including passive and active suicidal ideation, suicidal intent as well as suicidal behaviors. It rates an individual's degree of suicidal ideation on a scale, ranging from wish to be dead to active suicidal ideation with specific plan and intent. A higher number of yes responses indicated an increased degree of suicidal ideation.
Change in scores on 20-item Positive-Negative Affect Scale (PANAS)Baseline, 6 MonthsConsists of 10 positively and 10 negatively valanced word items. Items are rated by the participant for the extent they are feeling this right now on a scale of 1- slightly or not at all through 5- extremely. Total scores can range from 10-50, with higher scores representing higher levels of positive effect and lower scores having negative effect.
Change in scores on 20-item R-UCLA Loneliness ScaleBaseline, 6 MonthsA 20-item scale designed to measure one's subjective feelings of loneliness as well as feelings of social isolation. Participants rate each item on a scale from 1 (Never) to 4 (Often). A higher score indicates an increased degree of loneliness.
Change in scores on 14-item Mental Health Continuum Short Form (MHC-SF)Baseline, 6 MonthsConsists of 14 items and measures the degree of emotional well-being as defined in terms of positive affect/satisfaction with life; social well-being, social acceptance, social actualization, social contribution, social coherence social integration, psychological well-being, personal growth, positive relations with others, purpose in life and self-acceptance. Choices for these items vary between 1 to 7. Individuals who exhibit low levels (i.e., 'never' or 'once or twice' during the past month) on at least one measure of hedonic well-being and low levels on at least six measures of positive functioning are diagnosed with languishing mental health.
Change in scores on 12-item Flourishing Scale (FS)Baseline, 6 MonthsA measure of the participant's self-perceived success in relationships, self-esteem, purpose, and optimism. Items are rated on a seven point rating scale from 1 Strongly disagree to 7 Strongly agree. The scale provides a single psychological well-being score. A lower score indicates a decreased degree of well-being.
Change in scores on 8-item Grit-S scaleBaseline, 6 MonthsMeasures the individual's tendency to sustain interest in and effort toward very long-term goals. Eight items are assessed using a Likert-like scale (1 = Not like me at all, 5 = Very much like me). There are two sub-scales: Perseverance of Effort and Consistency of Interests. A lower score indicates a decreased decreased levels of perseverance and passion for long-term goals.
Change in scores on 10-item Life Orientation Test - RevisedBaseline, 6 MonthsMeasures positive and negative expectancies about future events. It consists of 20 statements referring to negative expectancies and 10 statements referring to positive expectancies. Participants answer on a 5-point scale (5 = I agree a lot, 1 = I DISagree a lot). A lower score indicates a decreased degree of life orientation.
Change in scores on 25-item Connor Davidson Resilience InventoryBaseline, 6 MonthsMeasures resilience. Range of scores (0-100). A score of 0 is suggestive of no resilience, a score of 100 is suggestive of high level of resilience.
Change in scores on 21-item Posttraumatic Growth InventoryBaseline, 6 MonthsSelf-reported measure of post-traumatic growth on a scale of 0 (Did not experience change as a result of their crisis) to 5 (experienced to a very great degree as a result of their crisis). A lower score indicates a decreased degree of posttraumatic growth.
11-item Effectiveness of Obtaining Resources scale (EOR)6 MonthsCalculates the mean of the effectiveness scores for obtaining resources from 11 different types of community resources including mental health treatment, church or clergy, health care, legal services, police, or social services.
Number of participants experiencing hospitalizations6 MonthsNumber of hospitalizations self-reported by participants during semi-structured interview. No or infrequent hospitalizations would indicate successful support for the participant via the RL app.
Number of participants experiencing self-injury events6 MonthsNumber of self-injury events reported during semi-structured interview. No or infrequent self-injury events would indicate successful support for the participant via the RL app.

Secondary

MeasureTime frameDescription
Number of participant reported barriers to care and resources16 WeeksThe number of participant reported barriers to care and resources will be gathered through mobile phone internal usage data coded and a semi-structured interview. Acceptance of ReliefLink as a treatment resource would be suggested if there aren't significant reported barriers.
Participant adherence to assigned coping skills activities16 WeeksThe frequency of Participant adherence to assigned coping skills activities will be gathered through mobile phone internal usage data coded and a semi-structured interview. Acceptance of ReliefLink as a treatment resource would be suggested if there was significant participant adherence.
Participant adherence to daily mood tracking16 WeeksThe degree of Participant adherence to daily mood tracking will be gathered through mobile phone internal usage data coded and a semi-structured interview. Acceptance of ReliefLink as a treatment resource would be suggested if there is significant adherence to mood tracking.
Participant usage of resource location functions16 WeeksThe frequency of Participant usage of resource location functions will be gathered through mobile phone internal usage data coded and a semi-structured interview. Acceptance of ReliefLink as a treatment resource would be suggested if is significant participant usage.
Participant positive feedback16 WeeksParticipant positive feedback will be gathered through a semi-structured interview. Acceptance of ReliefLink as a treatment resource would be suggested if there is positive participant feedback received.

Countries

United States

Outcome results

None listed

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