Skip to content

Effectiveness of a new social intervention to increase community connectedness and reduce isolation in adults transitioning home after long term hospital care: The Groups 4 Health Trial

Effectiveness of a new social intervention to increase community connectedness and reduce psychological distress in adults transitioning home after long term hospital care: The Groups 4 Health trial.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617001602314
Acronym
G4H Trial
Enrollment
121
Registered
2017-12-07
Start date
2015-04-20
Completion date
2017-02-20
Last updated
2017-12-16

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

Conditions

None listed

Brief summary

Social isolation is a major health risk and for many is associated with psychological distress. A new social group intervention, Groups 4 Health (G4H), has strong potential to address this problem. G4H is a five-module, manualized program that seeks to increase social connectedness by building group-based social identifications in the context of an in-vivo group experience. Its effectiveness has already demonstrated in a proof of-concept study (Haslam et al., 2016), but it has yet to be systematically trialled. This randomised controlled trial of G4H will recruit 130 adults presenting with psychological distress (i.e., elevated symptoms of depression or a mental health diagnosis) due to social isolation who will be randomly assigned to G4H or to a wait list control. The primary outcome against which the intervention will be assessed is loneliness and secondary outcomes include depression, social anxiety, and multiple group membership. We hypothesize a greater reduction in loneliness, depression, and anxiety and increase in multiple group membership for those receiving G4H compared to the wait list control.

Interventions

Groups 4 Health Trial: G4H is a manualized program that seeks to increase social connectedness by building group-based social identifications in the context of an in-vivo group experience. The five modules give people the knowledge and skills they need to manage their social group memberships, and the identities that underpin them, effectively. The intervention comprises 5 x 1.5 hour face-to-face group facilitated sessions, run weekly in the first month with the final module 5 delivered 1 mont

Groups 4 Health Trial: G4H is a manualized program that seeks to increase social connectedness by building group-based social identifications in the context of an in-vivo group experience. The five modules give people the knowledge and skills they need to manage their social group memberships, and the identities that underpin them, effectively. The intervention comprises 5 x 1.5 hour face-to-face group facilitated sessions, run weekly in the first month with the final module 5 delivered 1 month later. Modules 1-4 have associated homework after each session which takes about 30 minutes. The program is delivered in the Psychology Clinic of the School of Psychology, University of Queensland. Facilitators are Clinical and Health Psychology postgraduate students who receive training and weekly supervision to deliver the program. Module content is summarised below. Module 1: Schooling. Raises awareness of the beneficial effects that social group memberships have for health. It highlights the costs of ignoring the social dimensions of health and points out that failure to use all the social resources at our disposal generally leads to suboptimal health outcomes. The module also makes the point that it is within people’s power to counter these effects by learning how best to develop, maintain and harness group-based resources. Module 2: Scoping. Focuses on the range of group-based resources that people have, or ideally should have at their disposal, to optimize health. This module engages participants in the process of social identity mapping (Cruwys, Steffens, Haslam, et al., 2015). This tool was developed to explore respondents’ social identities, in order to assess their current social functioning and develop a sense of how they would ideally like to function in the futureIdentifying current group memberships and any gaps in group networks. Module 3: Sourcing. Targets development of skills needed to identify and strengthen existing valued social identities with a view to optimizing and sustaining these in the longer term. It also raises awareness of solutions to barriers to making the most of existing groups. Module 4: Scaffolding. Uses the G4H group as a model for establishing and embedding new social group connections whilst at the same time exploring strategies to identify which connections to develop and enact through a social plan of action. The goal is to trial these social plans between this and the final module, which takes place at least one month later. Module 5: Sustaining: Is a booster session held one month later that aims to troubleshoot any difficulties that have arisen in the course of implementing these social plans. It also revisits social identity maps, created in Module 2, to see how they have developed in the course of the program. The social foundations that have been identified and developed in the preceding four modules are also reviewed with a view to encouraging their long-term maintenance. In addition to the facilitator manual, the program is supported by a client workbook. This contains a summarized version of the facilitator’s manual highlighting the main activities and learning points for each session, with sufficient space to complete activities (both within the sessions and as homework) and document any relevant notes and plans to achieve particular goals. Treatment fidelity is assessed by brief questionnaire completed by facilitators at the end of each session delivered. This requires facilitators to tick off session activities covered, rate alliance and rapport between participants and with facilitator, indicate the length of session, and rate session satisfaction and ease of delivery.

Sponsors

University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Other
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Diagnosed with mental illness by health professional or 2. Scoring above the threshold (i.e., > 5) on the Patient Health Questionnaire - 9 (PHQ-9). 3. perceived social isolation

Exclusion criteria

1. known neurological condition 2. known history of psychosis 3. Unstable and fluctuating mental health condition that would interfere with taking part in a group program 4. severe learning impairment 5. non-English speaking

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026