Patient Partner Education Program 4 All after Resuscitation

Patient Partner Education Program 4 All after Resuscitation - PPEP4All-R

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON41058

Enrollment

120

Registered

2014-07-02

Start date

2014-04-01

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

hypoxic brain injury postanoxic encephalopathy

Interventions

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: minimum 1/2 year after cardiac arrest; survival after cardiac arrest; cognitive complaints objectified with MoCA, CFQ and IQCODE; age >=18 years;

Exclusion criteria

Exclusion criteria: patients: bad physical state; braindamage not due cardiac arrest; insufficient use of dutch language; restrictive behavioural problems;affecting psychiatric comorbidity;partners: restrictive behavioural problems; insufficient use of Dutch langauge; bad physical state

Design outcomes

Primary

Measure	Time frame
Primary study parameter is the quality of life (SF-36) of the patients and the experienced strain of the caregiver (Caregiver Strain Index).	—

Secondary

Measure	Time frame
Clinical outcomes are: • Experienced cognitive complaints(Cognitive Failure Questionnaire), • Experienced cognitive changes by the spouse/care giver (Informant Questionnaire on Cognitive Decline in the Elderly), • Effects towards autonomy and partipation (Impact on Participation and Autonomy) • Severity of fear and derpession (Hospital Anxiety and Depression Scale) • Amount of care of patients and caregiver/spuse (focus group) • Cognitive functioning (Montreal Cognitive Assessment) outcomes process: • Satisfaction of patient, partner and trainer towards the followed/given intervention (Visual Analoge Scale) • Any necessary modifications made in the existing PPEP4All workbooks and meetings.	—

Measure

Time frame

Clinical outcomes are: • Experienced cognitive complaints(Cognitive Failure Questionnaire), • Experienced cognitive changes by the spouse/care giver (Informant Questionnaire on Cognitive Decline in the Elderly), • Effects towards autonomy and partipation (Impact on Participation and Autonomy) • Severity of fear and derpession (Hospital Anxiety and Depression Scale) • Amount of care of patients and caregiver/spuse (focus group) • Cognitive functioning (Montreal Cognitive Assessment) outcomes process: • Satisfaction of patient, partner and trainer towards the followed/given intervention (Visual Analoge Scale) • Any necessary modifications made in the existing PPEP4All workbooks and meetings.

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Countries

Netherlands

Outcome results