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Effect of a Brief Psychological Intervention on Anxiety and Depression During COVID-19

Randomised Controlled Trial of Brief Psychological Intervention versus Supportive Counseling on Anxiety and Depression in Indian Students Distressed by COVID-19

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621001064897
Enrollment
183
Registered
2021-08-12
Start date
2021-10-10
Completion date
2022-12-05
Last updated
2024-10-28

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

Conditions

None listed

Brief summary

The global impact of COVID-19 has been profound, and the public health threat it represents is the most serious seen in recent pandemic history. Thus, concerns about COVID-19 are pervasive and have several serious adverse impacts on the mental health of health workers and the general community. There is an urgent demand for programs that can address the stress experienced by people during the COVID-19 pandemic. This situation does not require therapy because these personnel do not necessarily suffer from a mental disorder. Instead, there are huge numbers of people who are facing unprecedented levels of stress and require strategies to manage this stress. One of the key groups of people who are highly distressed during the pandemic are university students because of the financial, academic, and social pressures on them. The UNSW team has developed suitable and evidence-based program that helps to cope with stress during the pandemic. As a low-intensity intervention for adults affected by the pandemic, this program teaches people well-documented strategies to manage stress. This project aims to conduct a rapid trial of a brief psychological intervention, termed Coping with COVID to reduce distress in Indian university student associated with concerns about COVID-19. There is an urgent need for publicly available strategies to reduce COVID-19 related distress. This project does not aim to treat a mental disorder but rather alleviate distress and improve coping in people with distress about COVID-19. This brief program will be offered via teleconferencing to allow for social distancing on a group basis. We hypothesise that Coping with COVID will result in greater reductions in anxiety and depression elative to supportive counselling. Adults who screen positive for psychological distress will be randomized to Coping with COVID or supportive counseling via teleconferencing to groups of 4 people at a time. The control arm will provide 6 peer-led supportive counseling sessions delivering in groups of 4 people via video-conferencing. All participants will be assessed at baseline, post-intervention, and 2 and 6 months follow-up

Interventions

There are two arms to this trial that were designed specifically for this trial. Arm 1: Psychological Intervention. Arm 2: Supportive Counselling. Therapy is administered once-weekly 60 minute sessions by peers with 3 or 4 years of undergraduate education over 6 weeks delivered via teleconferencing to groups of 4 people at a time. The intervention teaches participants the following stress coping strategies: anxiety reduction, problem solving, behavioral activation, and accessing social support.

There are two arms to this trial that were designed specifically for this trial. Arm 1: Psychological Intervention. Arm 2: Supportive Counselling. Therapy is administered once-weekly 60 minute sessions by peers with 3 or 4 years of undergraduate education over 6 weeks delivered via teleconferencing to groups of 4 people at a time. The intervention teaches participants the following stress coping strategies: anxiety reduction, problem solving, behavioral activation, and accessing social support. This will occur will via group discussions via teleconference. Treatment adherence will be assessed by checklist completed by facilitators. The duration of the study for any participant will conclude after a 6-month follow-up assessment, resulting in participation duration of 33 weeks.

Sponsors

UNSW Sydney
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

Inclusion Criteria: • Score of greater than or equal to 16 on the K10 • Aged at least 18 years • University student • Sufficient English language comprehension • Access to teleconferencing platform

Exclusion criteria

Exclusion Criteria: • Current psychosis • Imminent suicidal risk • Current substance dependence No access to internet-based access to teleconferencing facility

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 12, 2026