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A randomised controlled trial of an intervention to improve communication with patients suffering acute chest pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN85248020
Enrollment
720
Registered
2005-11-28
Start date
2005-11-15
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Acute chest pain Signs and Symptoms Chest pain

Interventions

Chest pain from suspected heart disease is a common cause for emergency hospital attendance. Despite receiving a thorough investigation, many patients report anxiety, poor health and concerns regardin

Sponsors

The University of Sheffield (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients presenting to the Emergency Department with acute chest pain who are subsequently managed on the Chest Pain Unit (CPU) will be eligible for inclusion in the study: phase 1 and 2.

Exclusion criteria

Exclusion criteria: Patients who are unable to read or understand the trial will be excluded.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be score on the anxiety scale of the Hospital Anxiety and Depressions Scale (HADS).

Secondary

MeasureTime frame
1. HADS depression score 2. 36-item Short Form health survey (SF-36) scores 3. Patient satisfaction 4. Proportion with persistent chest pain at one month 5. Proportion who have attempted/succeeded in smoking cessation 6. Dietary change or increased exercise 7. A 'knowledge score' regarding their complaint Planned subgroup analyses will compare outcomes for the following subgroups: 1. Patients with a final diagnosis of angina 2. Patients with an uncertain diagnosis 3. Patients with benign (non-cardiac) chest pain

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026