Effects of treating exhaustion in angioplasty patients on new coronary events: Results of the Randomized Exhaustion Trial (EXIT).

Randomized Exhaustion Intervention Trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON29223

Enrollment

710

Registered

2005-09-13

Start date

1996-07-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

1. Behavioural intervention including relaxation therapy

Interventions

1. Behavioural intervention including relaxation therapy

2. Ususal care.

Eligibility

Inclusion criteria

Inclusion criteria: Exhausted patients being treated successfully with PCI (reduction in stenosis of >50%).

Exclusion criteria

Exclusion criteria: 1. Severe somatic or mental comorbidity; 2. Somtization disorder, fibromyalgia or chronic fatigue; 3. Participation in a behavioural, rehabilitation program other than EXIT; 4. Unsuccessful treatment for a recent depression or panic disorder; 5. Inability to speak Dutch.

Design outcomes

Primary

Measure	Time frame
1. Exhaustion; 2. New coronary event, 'de novo' lesions - all at 18 months follow-up.	—

Secondary

Measure	Time frame
New coronary events (6 months).	—

Contacts

Public ContactJ.K.L. Denollet

Tilburg University, Department of Psychology and Health, P.O. Box 90153

denollet@uvt.nl+31 (0)13 4662390

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)