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Improving the effectiveness of psychological interventions for depression and anxiety in the cardiac rehabilitation pathway: a single-blind randomised controlled trial

Improving the effectiveness of psychological interventions for depression and anxiety in the cardiac rehabilitation pathway: a single blind randomised controlled trial with four month and twelve month follow up comparing GroupMCT plus usual CR (intervention) with usual CR (control).

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN74643496
Enrollment
332
Registered
2015-04-08
Start date
2015-06-01
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Topic: Cardiovascular disease

Interventions

1. Experimental: metacognitive therapy plus CR Group psychological treatment focused on reducing worry and rumination and modifying beliefs about thinking in addition to treatment as usual (standard c

Sponsors

Manchester Mental Health & Social Care Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Heart disease patients referred to CR who meet DoH and/or BACPR CR eligibility criteria 2. Minimum of 18 years old 3. Competent level of English language skills (able to read, understand and complete questionnaires in English). 4. Acute coronary syndrome used for any condition brought on by sudden, reduced blood flow to the heart 5. Following revascularisation is the restoration of perfusion to a body part or organ that has suffered ischemia 6. Stable heart failure 7. Stable angina is chest pain or discomfort that most often occurs with activity or stress 8. Following implantation of cardioverter defibrillators/cardiac resynchronisation devices 9. Heart valve repair/replacement 10. Heart transplantation and ventricular assist devices 11. Adult congenital heart disease identified in adulthood 12. A score of = 8 on either the depression or anxiety subscale of the HADS.

Exclusion criteria

Exclusion criteria: 1. Cognitive impairment which precludes informed consent or ability to participate 2. Acute suicidality 3. Active psychotic disorders (i.e., two [or more] of the following: delusions, hallucinations, disorganized speech, grossly disorganized or catatonic behaviour, negative symptoms) 4. Current drug/alcohol abuse a maladaptive pattern of drinking, leading to clinically significant impairment or distress 5. Concurrent psychological intervention for emotional distress 6. Antidepressant or anxiolytic medications initiated in the previous 8 weeks 7. Life expectancy of less than 12 months

Design outcomes

Primary

MeasureTime frame
Change in Hospital Anxiety and Depression Scale (HADS) [Time Frame: Baseline pre treatment, four-month post baseline, 12 months follow-up]

Secondary

MeasureTime frame
1. Metacognitions Questionnaire 2. Cognitive Attentional Syndrome 3. Impact of Event Scale-Revised 4. Health Related Quality of Life 5. Economic Patient Questionnaire (EPQ)

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 7, 2026