The evaluation of a group therapy for patients with depressive symptoms after stroke - a pilot study

The evaluation of a group therapy for patients with depressive symptoms after stroke - a pilot study - Evaluation of a group therapy for depressive symptoms after stroke

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON29896

Enrollment

Registered

2006-07-07

Start date

2006-04-10

Completion date

Unknown

Last updated

2024-06-18

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

Conditions

Depressive symptoms

Interventions

The *Coping with depressive symptoms after stroke* course is a stroke adapted version of the *Coping with depression* course Dutch version by Cuijpers (1995). The course is expanded to give more att

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: -he/she is receiving treatment in the HRC for stroke -he/she has sufficient cognitive abilities to follow the intervention, based on clinical judgement of a psychologist, with a Mini Mental State Examination score at least higher than 15 -he/she reports at least one emotional complaint on the CheckList for Cognitive and Emotional Consequences of Stroke (CLCE-24) -he/she is at least 18 years old

Exclusion criteria

Exclusion criteria: -insufficient understanding of the Dutch language -severe aphasia -insufficient physical abilities -serious vision or hearing problems -little or no insight into physical functioning, based on clinical judgement -co-morbid neurological disorders other than stroke -suffer or have suffered from a serious psychiatric disorder in the last five years for which he/she is treated for more than half a year by a psychiatrist -he/she did not give permission

Design outcomes

Primary

Measure	Time frame
The study parameters are mood, depressive symptoms and health related quality of life.	—

Secondary

Measure	Time frame
nvt	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)