Psycho-Education Physical Exercise Effects: does treating subsyndromal depression improve depression- and diabetes-related outcomes?

ISRCTN ISRCTN05673017
DOI https://doi.org/10.1186/ISRCTN05673017
Secondary identifying numbers 091410
Submission date
27/07/2010
Registration date
11/08/2010
Last edited
09/09/2015
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Nutritional, Metabolic, Endocrine
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English Summary

Not provided at time of registration

Contact information

Dr Mirjana Pibernik-Okanovic
Scientific

Vuk Vrhovac University Clinic
Zagreb
10000
Croatia

Phone +385 (0)1 235 3935
Email mirjana.pibernik@idb.hr

Study information

Study designRandomised controlled three-arm study
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Hospital
Study typeTreatment
Participant information sheet Not available in web format, please use the contact details below to request a patient information sheet
Scientific titleA randomised controlled comparison of psycho-education, physical exercise and treatment as usual in patients with diabetes and suffering from subsyndromal depression
Study acronymPEPEE
Study hypothesisEarly treatment of subsyndromal depression in patients with diabetes is expected to improve the patients' depressive symptoms and health status including indicators of metabolic control, subjectively perceived quality of life, diabetes-related distress and diabetes self-care.
Ethics approval(s)Ethics Committee of the Vuk Vrhovac University Clinic, 01/07/2010
ConditionType 2 diabetes/subsyndromal depression
Intervention1. Psycho-educational intervention:
The intervention will comprise 6 interactive small-group meetings (4 - 6 members), each lasting for 60 - 90 minutes. The topics will include:
1.1. Symptoms of depression, interaction of depression and diabetes
1.2. Alleviating burden of depression through activities and problem solving
1.3. Associations between depression and cognitive processes - thoughts, beliefs and attitudes that induce and maintain depression, and developing a personal plan for managing problems in the future

The meetings will be held at weekly intervals. Patients will be provided with a self-help manual for overcoming depressive difficulties based on the "Coping with depression" course by P.M. Lewinsohn. The manual will be given to the participating patients prior to the first session in order to make them familiar with the course and to facilitate reflecting their own experiences. The manual's structure aims to stimulate introducing personal examples and making notes. The "Coping with depression" program is well-evaluated in both general population and medical patients. For the purpose of this study the program has been modified in two ways: it has been adjusted to address specific emotional problems related to diabetes, and also adapted for a shorter format of this intervention. Patients will also receive a workbook containing exercises to recognize depressive symptoms, become aware of daily activities patterns, acquire problem-solving techniques, and to recognize and modify cognitive patterns that contribute to maintenance of depression. The manual was tested for comprehensibility and clarity in a group of diabetic patients (N = 8) with different demographic and disease-related characteristics.

2. Physical activity intervention:
The intervention will comprise 6 small-group weekly sessions. The purpose of these sessions will be to educate patients about the interaction of physical activity, mood and diabetes and to increase their participation in a variety of physical activities with an emphasis on walking. The sessions will combine interactive lectures and exercise techniques (warm up-flexibility, strengthening and stretching exercises) that are considered suitable for the study participants. The educational topics will include:
2.1. Effects of exercise on mood
2.2. Short- and long-term effects of exercise on blood glucose and cardiovascular system
2.3. Strategies to develop and maintain a personal plan for regular exercise. The program has been developed by a professional trainer experienced in working with the diabetic population.

The sessions will be organised in a group format and led by a professional trainer. Exercise intensity will be measured by a cardiosport watch. The volume of physical activity will be monitored by a pedometer for one week preceding each point of measurement.

3. Depression screening followed by diabetes treatment as usual:
The patients screened for depression will be given an explanation of their result and informed about available treatment options. Follow-up data will be collected at the same points of measurement as in the treatment groups.

The total duration of the treatments (psycho-education; physical exercise) is six weeks. A one-year follow-up has been planned for all three arms of the trial.
Intervention typeOther
Primary outcome measureDepressive symptoms, measured after the treatment (i.e. after six weeks for the "diabetes treatment as usual" group), and after six- and twelve-month follow-up periods.
Secondary outcome measures1. Self-management of diabetes, measured at six weeks for the "diabetes treatment as usual" group, and after six- and twelve-month follow-up periods
2. Metabolic control, measured at six weeks for the "diabetes treatment as usual" group, and after six- and twelve-month follow-up periods
3. Diabetes-related distress, measured at six weeks for the "diabetes treatment as usual" group, and after six- and twelve-month follow-up periods
4. Health-related quality of life, measured at six weeks for the "diabetes treatment as usual" group, and after six- and twelve-month follow-up periods
5. Treatment satisfaction, measured after the treatment
Overall study start date01/09/2010
Overall study end date01/09/2013

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexBoth
Target number of participants59 participants per group
Participant inclusion criteria1. Type 2 diabetes
2. Aged 18 - 60 years, either sex
3. Subsyndromal depression as determined by the screenings instruments (Patient Health Questionnaire-2 [PHQ-2], Center for Epidemiologic Studies Depression Scale [CES-D]) and the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID)
4. Willing to participate (signing a written informed consent)
Participant exclusion criteria1. Poor literacy
2. Mobility difficulties
3. Visual impairment
4. Drinking problems
5. Psychosis in personal medical history
6. Medical contraindications for physical exercise (heart attack or stroke in the past six months, chest pain, dizziness, fainting attacks, shortness of breath)
Recruitment start date01/09/2010
Recruitment end date01/09/2013

Locations

Countries of recruitment

  • Croatia

Study participating centre

Vuk Vrhovac University Clinic
Zagreb
10000
Croatia

Sponsor information

European Foundation for the Study of Diabetes (EFSD) (Germany)
Charity

Rheindorfer Weg 3
Duesseldorf
40591
Germany

Phone +49 (0)211 758469 0
Email Foundation@easd.org
Website http://www.EuropeanDiabetesFoundation.org
ROR logo "ROR" https://ror.org/05tgz4m05

Funders

Funder type

Charity

European Foundation for the Study of Diabetes (EFSD) (Germany)
Private sector organisation / Trusts, charities, foundations (both public and private)
Alternative name(s)
The European Association for the Study of Diabetes, EFSD
Location
Germany

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Protocol article protocol 21/01/2011 Yes No
Results article results 01/07/2015 Yes No
Results article results 15/07/2015 Yes No