Ignite Creation Date:
2024-05-06 @ 1:13 AM
Last Modification Date:
2024-10-26 @ 11:01 AM
Study NCT ID:
NCT01765725
Status:
COMPLETED
Last Update Posted:
2017-10-16
First Post:
2013-01-04
Brief Title:
Coping With Chronic Fatigue Syndrome Development of a Community-based Patient Education Program
Sponsor:
Oslo University Hospital
Organization:
Oslo University Hospital
Study Overview
Official Title:
Coping With Chronic Fatigue Syndrome Development of a Community-based Patient Education Program
Status:
COMPLETED
Status Verified Date:
2017-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of the study is to develop carry out evaluate and measure the effects of a new patient education program for patients with Chronic Fatigue Syndrome CFSin primary healthcare
In an randomized controlled trial design the effects of the patient education program on coping physical functioning fatigue pain acceptance anxiety depression quality of life self- efficacy and illness perception will be compared with treatment as usual
The results of the main project will lead to the elaboration of the final patient education program that can be implemented in primary health care as well as development of a training program for future program-conductors
In an randomized controlled trial design the effects of the patient education program on coping physical functioning fatigue pain acceptance anxiety depression quality of life self- efficacy and illness perception will be compared with treatment as usual
The results of the main project will lead to the elaboration of the final patient education program that can be implemented in primary health care as well as development of a training program for future program-conductors
Detailed Description:
The project is a single blind randomized controlled trial A total of 150 participants will be included in this study and randomly allocated to the intervention- or the control group The 75 participants in the intervention group will be allocated to 6 groups The control group will be offered to take part in the patient education program as soon as they have completed the last outcome evaluations
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 36IAJ3 | OTHER_GRANT | Extra Stiftelsen Helse og Rehabilitering | None |
| 2011894REK nord | REGISTRY | None | None |