Trial Outcomes & Findings for Prognosis of Depression in the Elderly (PRODE). A Multicentre, Longitudinal Study of Elderly Depressed Patients. (NCT NCT01952366)
NCT ID: NCT01952366
Last Updated: 2026-04-13
Results Overview
Relapse/recurrence of depression
COMPLETED
169 participants
1 year after inclusion to the study
2026-04-13
Participant Flow
Participant milestones
| Measure |
Depressed Patients
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Overall Study
STARTED
|
169
|
|
Overall Study
COMPLETED
|
138
|
|
Overall Study
NOT COMPLETED
|
31
|
Reasons for withdrawal
| Measure |
Depressed Patients
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Overall Study
Death
|
22
|
|
Overall Study
Withdrawal by Subject
|
9
|
Baseline Characteristics
Prognosis of Depression in the Elderly (PRODE). A Multicentre, Longitudinal Study of Elderly Depressed Patients.
Baseline characteristics by cohort
| Measure |
Depressed Patients
n=169 Participants
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=193 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
6 Participants
n=193 Participants
|
|
Age, Categorical
>=65 years
|
163 Participants
n=193 Participants
|
|
Age, Continuous
|
76.1 years
STANDARD_DEVIATION 6.8 • n=193 Participants
|
|
Sex: Female, Male
Female
|
123 Participants
n=193 Participants
|
|
Sex: Female, Male
Male
|
46 Participants
n=193 Participants
|
|
Region of Enrollment
Norway
|
169 participants
n=193 Participants
|
PRIMARY outcome
Timeframe: 1 year after inclusion to the studyPopulation: Inpatients
Relapse/recurrence of depression
Outcome measures
| Measure |
Depressed Patients
n=146 Participants
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Depression
|
48 participants
|
PRIMARY outcome
Timeframe: Three years follow-up (mean follow-up time: 1167 days (SD=41)We have described the course of depression after treatment in departments of old-age psychiatry at specialist healthcare services using assessments at one- and year follow-up. The patients were decribed in the following categories courses: Favourable/less favourable/unfavourable/unclassifiable.
Outcome measures
| Measure |
Depressed Patients
n=131 Participants
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Depression During Three Years
Favourable course
|
24 Counts of participants
|
|
Depression During Three Years
Less favourable course
|
55 Counts of participants
|
|
Depression During Three Years
Unfaourable course
|
51 Counts of participants
|
|
Depression During Three Years
Unclassifiable
|
1 Counts of participants
|
SECONDARY outcome
Timeframe: 1 year after inclusion to the studyOne year after inclusion to the study, there will be a clinical assessment of the patient including a MMSE, if possible, and to evaluate if the patients have dementia.
Outcome measures
| Measure |
Depressed Patients
n=146 Participants
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Number of Patients With a Diagnosis of Dementia (According to ICD-10) One Year After Inclusion to the Study.
|
23 Participants
|
SECONDARY outcome
Timeframe: 3 years after inclusion to the study (mean time 1167 days, SD 41).3 years after inclusion to the study there was an assessment inluding all available information on cognition; i.e. information from previous follow-ups, clinical or telephone assessment of cognition using Mini Mental Status Examination (MMSE, clinical or telephone-version), and information from next-of-kin or caregivers including the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) and The Clinical Dementia Rating (CDR). Three Senior Consultants with a PhD then used all available information to diagnose dementia according to the ICD-10 classification.
Outcome measures
| Measure |
Depressed Patients
n=131 Participants
Patients admitted to specialist health care service of old age psychiatry
|
|---|---|
|
Number of Patients With a Diagnosis of Dementia (According to ICD-10) Three Years After Inclusion to the Study.
|
40 Count of participants
|
Adverse Events
Depressed Patients
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place