search
Back to results

The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation (DOPPELHERZ)

Primary Purpose

Coronary Artery Disease

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
traditional cardiac rehabilitation
combined exercise
Sponsored by
Technical University of Munich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Coronary Artery Disease

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • participation in cardiac rehabilitation
  • written consent
  • < 1.4 watt/kgBW exercise capacity not more than 12 weeks before study begin

Exclusion Criteria:

  • >= 1.4 watt/kgBW
  • contraindications to exercise participation
  • hospitalized for CVD within six weeks of inclusion
  • acute illness/injury (e.g. fever)
  • chronic drug abuse
  • inability to understand study instructions
  • unwillingness to participate

Sites / Locations

  • Klinikum rechts der Isar/ Technische Universitaet Muenchen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

combined exercise

traditional cardiac rehabilitation

Arm Description

90 minutes combined endurance and resistance exercise once a week plus 90 minutes traditional cardiac rehabilitation once a week over six months

The group-based program is offered for 90 minutes twice a week and is a combination of gymnastics, coordination and flexibility exercises, and includes educational components targeting diet and nutrition, stress and relaxation, methods for coping with CVD and behavioral and lifestyle change.

Outcomes

Primary Outcome Measures

Change from baseline in maximal exercise capacity (watt/kgBW)

Secondary Outcome Measures

Change from baseline in maximal exercise capacity (watt/kgBW)
Change from baseline in anthropometric measures
Change from baseline in waist to hip circumference ratio, body mass index, percent body fat and weight.
Change from baseline in Health Relates Quality of Life (HRQoL as measured by questionnaires)
Questionnaires used: Short From 36 (SF-36), Global Mood Scale (GMS), MacNew Heart Disease Quality of Life Instrument (MacNew)
Number of patients with adverse events (AE; documented)
Change in clinical symptoms (NYHA-stage, CCS-stage, number, type and dose of medications))
Change in physical activity level (based on 7-day accelerometry)
Patients will wear accelerometers for 7 days at baseline, 6 months and 12 months, and the change in physical activity level will be calculated
Change from baseline in upper and lower body muscular strength (1RM; kg)
Upper and lower body muscular strength will be measured using a chest press and a leg extension device, respectively.
Change from baseline in anthropometric measures
Change from baseline in waist to hip circumference ratio, body mass index (BMI), percent body fat (%) and weight (kg).
Change from baseline in blood pressure (Systolic and Dystolic;mmHg)
24-hour blood pressure will be measured using a holter BP monitor

Full Information

First Posted
July 5, 2013
Last Updated
January 22, 2015
Sponsor
Technical University of Munich
search

1. Study Identification

Unique Protocol Identification Number
NCT01921036
Brief Title
The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation
Acronym
DOPPELHERZ
Official Title
Individuell Dosiertes Kraft-ausdauer-training in Ambulanten Herzgruppen - Einfluss Auf Koerperliche Belastbarkeit Von Herzpatienten.
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
January 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Technical University of Munich

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Seventy patients in cardiac rehabilitation with maximal exercise capacity less than 1.4 watt per kilogram bodyweight will be randomized 1:1 into either an intervention training (IN) group or usual care (UC). The IN patients will perform supervised endurance and resistance exercise for approximately 90 minutes once a week and traditional cardiac rehabilitation (TCR) once a week; the UC patients will perform TCR twice a week. The intervention is planned for six months with a follow-up of a further six months. The primary investigation is differences between IN and UC with regard to changes in exercise capacity (max watt/kgBW).
Detailed Description
The DOPPELHERZ (The influence of individualized resistance-endurance exercise training on maximal power output in outpatient cardiac rehabilitation) randomized controlled trial was performed at the Department of Prevention and Sports Medicine, Klinikum rechts der Isar in Munich, Germany. 70 patients eligible for and/or participating in cardiac rehabilitation were randomized to six months in an individualized combined exercise group (ICE) or group- based cardiac rehabilitation (GCR), considered usual care in this patient population. All patients gave written informed consent, the study protocol was approved by the local university hospital ethics committee, all procedures were conducted according to the Declaration of Helsinki. Participants: All patients were American Heart Association Class "C" (moderate to high risk) based on the presence of cardiac disease and maximal power output of <5 METs (corresponding to <1.4 W/kg body weight), who met eligibility criteria for CR at the time of recruitment. Patients with decompensated or highly symptomatic (NYHA IV) heart failure, acute illness or injury, cardiac hospitalizations within six weeks of inclusion, drug abuse, unstable blood pressure or arrhythmias, high grade valve stenosis or instable diabetes mellitus were excluded. Primary endpoint: The primary endpoint was change in maximal relative power output (W/kg) measured by CPX after six months. Exercise training program In both the intervention and usual care arms of the study, exercise training was prescribed twice weekly over a period of six months, and all exercise sessions were led by certified exercise instructors and monitored by physicians. Group-based cardiac rehabilitation (GCR): The GCR group performed regular exercise in a state-sanctioned cardiac rehabilitation group. This form of GCR is considered Phase III aftercare and has been described elsewhere9. Briefly, GCR patients received moderate-intensity heart rate targets from exercise cardiologists based on CPX results. The group-based program is offered for 90 minutes twice a week and is a combination of gymnastics (including endurance and resistance components), coordination and flexibility exercises, and includes educational components targeting diet and nutrition, stress and relaxation, methods for coping with CVD and behavioral and lifestyle change. The GCR sessions were conducted at a local university gymnasium and were performed in groups of up to 15 participants, as recommended by the German Federal Association for Rehabilitation. Individualized combined exercise (ICE): The ICE group participated in once-weekly individualized combined resistance-endurance exercise training for 60 minutes and once-weekly traditional group-based cardiac rehabilitation as described above. The ICE intervention included 30 minutes of endurance exercise at 60-70% VO2peak and RPE 11-14 and five resistance exercises (chest press, leg press, lat pull-downs, shoulder press and seated cable row) following the recommendations of the German Federation for Cardiovascular Prevention and Rehabilitation (DGPR) and targeting the large muscle groups at an RPE<16. For the first three months, patients performed two sets of 12-25 repetitions at 30-50% 1RM; after three months patients were retested and thereafter performed two sets of 8-15 repetitions at 40-60% 1RM. The ICE sessions were located at the university sports medicine rehabilitation center and performed in groups of not more than four patients. They were instructed at a maximum 2:1 participant to therapist ratio.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
combined exercise
Arm Type
Experimental
Arm Description
90 minutes combined endurance and resistance exercise once a week plus 90 minutes traditional cardiac rehabilitation once a week over six months
Arm Title
traditional cardiac rehabilitation
Arm Type
Active Comparator
Arm Description
The group-based program is offered for 90 minutes twice a week and is a combination of gymnastics, coordination and flexibility exercises, and includes educational components targeting diet and nutrition, stress and relaxation, methods for coping with CVD and behavioral and lifestyle change.
Intervention Type
Procedure
Intervention Name(s)
traditional cardiac rehabilitation
Intervention Description
mutifactoral cardiac rehabilitation
Intervention Type
Procedure
Intervention Name(s)
combined exercise
Intervention Description
Moderate endurance and resistance exercise once a week over six months
Primary Outcome Measure Information:
Title
Change from baseline in maximal exercise capacity (watt/kgBW)
Time Frame
six months
Secondary Outcome Measure Information:
Title
Change from baseline in maximal exercise capacity (watt/kgBW)
Time Frame
12 months
Title
Change from baseline in anthropometric measures
Description
Change from baseline in waist to hip circumference ratio, body mass index, percent body fat and weight.
Time Frame
six and 12 months
Title
Change from baseline in Health Relates Quality of Life (HRQoL as measured by questionnaires)
Description
Questionnaires used: Short From 36 (SF-36), Global Mood Scale (GMS), MacNew Heart Disease Quality of Life Instrument (MacNew)
Time Frame
six and 12 months
Title
Number of patients with adverse events (AE; documented)
Time Frame
six and 12 months
Title
Change in clinical symptoms (NYHA-stage, CCS-stage, number, type and dose of medications))
Time Frame
six and 12 months
Title
Change in physical activity level (based on 7-day accelerometry)
Description
Patients will wear accelerometers for 7 days at baseline, 6 months and 12 months, and the change in physical activity level will be calculated
Time Frame
six and 12 months
Title
Change from baseline in upper and lower body muscular strength (1RM; kg)
Description
Upper and lower body muscular strength will be measured using a chest press and a leg extension device, respectively.
Time Frame
six and 12 months
Title
Change from baseline in anthropometric measures
Description
Change from baseline in waist to hip circumference ratio, body mass index (BMI), percent body fat (%) and weight (kg).
Time Frame
six and 12 months
Title
Change from baseline in blood pressure (Systolic and Dystolic;mmHg)
Description
24-hour blood pressure will be measured using a holter BP monitor
Time Frame
6 and 12 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: participation in cardiac rehabilitation written consent < 1.4 watt/kgBW exercise capacity not more than 12 weeks before study begin Exclusion Criteria: >= 1.4 watt/kgBW contraindications to exercise participation hospitalized for CVD within six weeks of inclusion acute illness/injury (e.g. fever) chronic drug abuse inability to understand study instructions unwillingness to participate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey W Christle, M.A.
Organizational Affiliation
Klinikum rechts der Isar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Klinikum rechts der Isar/ Technische Universitaet Muenchen
City
Munich
ZIP/Postal Code
80992
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

The Effects of Combined Exercise Training on Exercise Capacity in Cardiac Rehabilitation

We'll reach out to this number within 24 hrs