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Managing depression and anxiety risk in those with cardiovascular disease - A nurse led intervention

A pilot study of a nurse-led Intervention that will facilitate the modification of health related behaviours through motivational interviewing and further education on self care strategies in patients at risk of depression and anxiety following an acute cardiac event.

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000077864
Enrollment
100
Registered
2012-01-16
Start date
2012-02-01
Completion date
Unknown
Last updated
2020-01-13

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 proposed project will introduce a Nurse Led Intervention (NLI) to engage patients with an admission for cardiovascular disease (CVD) and co-morbid depression and or anxiety. The NLI will facilitate the modification of health related behaviours through motivational interviewing and further education on self care strategies.

Interventions

Managing depression and anxiety in cardiovascular patients via Motivational interviewing. There will be an initial one hour nurse led consultation followed by weekly 15-30 minute telephone calls for the first month, then fortnightly for the next month. At 3 months, participants will be invited to attend a second face-to-face consultation with the nurse. After the second consultation the participant will have monthly follow up calls for the next two months and a final face-to face consultation a

Managing depression and anxiety in cardiovascular patients via Motivational interviewing. There will be an initial one hour nurse led consultation followed by weekly 15-30 minute telephone calls for the first month, then fortnightly for the next month. At 3 months, participants will be invited to attend a second face-to-face consultation with the nurse. After the second consultation the participant will have monthly follow up calls for the next two months and a final face-to face consultation at 6 months

Sponsors

Australian Catholic University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

*Primary diagnosis of one or more of the following atherosclerotic related events acute coronary syndrome, coronary artery bypass grafts, stroke, transient ischemic attack, or peripheral vascular disease. * Aged 18 and above * Telephone access * HADS score = / >11 * Fluent in English

Exclusion criteria

* Diagnosed with a terminal illness * Cognitive impairment that may impact upon ability to participate in the trial * Participant is housebound * Existing diagnosis of a psychiatric condition including bipolar illness, psychotic illness, dementia, severe personality disorder * Dependence on alcohol or other substances other than nicotine * Participation in other research trial that may interfere with the trial * Inability to give informed consent * Any other factor impacting upon ability to give informed consent or participate in the study

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026