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Isometric Muscle Training in Patients With Spinal Bony Metastases Under Radiation Therapy (DISPO)

Primary Purpose

Vertebral Bony Metastases

Status
Completed
Phase
Phase 2
Locations
Germany
Study Type
Interventional
Intervention
exercise
Sponsored by
Heidelberg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vertebral Bony Metastases focused on measuring bony metastases, physical exercise

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • solitary or multiple vertebral metastases
  • thoracic spine
  • lumbar spine
  • sacrum
  • indication for palliative radiation therapy
  • age: 18 - 80 years
  • Karnofsky index > 70%
  • bisphosphonate therapy inititated

Exclusion Criteria:

  • bony metastases of cervical spine or pelvis
  • impending fracture
  • other serious illnesses or medical conditions: therapy-refractory unstable heart disease, congestive heart failure NYHA °III and °IV; coagulopathies
  • Significant neurological or psychiatric condition including dementia or seizures or other serious medical condition prohibiting the patient's participation in the trial by judgement of the investigators
  • Legal incapacity or limited legal capacity
  • Positive serum/ urine beta-HCG/ pregnancy

Sites / Locations

  • Dept of Radiation Oncology, University of Heidelberg, Germany

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

A

B

Arm Description

patients in arm A carry out daily physical training consisting of three different isometric exercises under the guidance and supervision of a physiotherapist. Training starts day one (first radiotherapy session), 10 daily units of 30 min each are scheduled during radiotherapy. Patients are expected to continue training until 12 weeks post completion of radiotherapy at home.

Patients in arm B (control group) receive 10 daily sessions of 15 min manual therapy (i.e. massage, etc) starting from day one of radiotherapy.

Outcomes

Primary Outcome Measures

feasibility of isometric exercise in vertebral bony metastases
safety and feasibility of isometric exercise in vertebral bony metastases

Secondary Outcome Measures

progression-free survival (PFS)
PFS is assessed 2 years post completion of radiotherapy
fracture-free survival (FFS)
FFS is assessed 2 years post completion of radiotherapy
bone density
bone density is assessed 12 weeks post completion of radiotherapy using follow-up CT scan of the spine
pain reduction
pain is evaluated using the VAS pain scale (0-100 points) at completion and 12/ 24 weeks post completion of radiation therapy
Quality of life
Quality of life is assessed using the EORTC BM22 questionnaire at 12 and 24 weeks post completion of treatment
Fatigue
Fatigue is assessed using the EORTC FA13 questionnaire

Full Information

First Posted
August 2, 2011
Last Updated
March 19, 2014
Sponsor
Heidelberg University
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1. Study Identification

Unique Protocol Identification Number
NCT01409720
Brief Title
Isometric Muscle Training in Patients With Spinal Bony Metastases Under Radiation Therapy
Acronym
DISPO
Official Title
Isometric Muscle Training of the Spine Musculature in Patients With Spinal Bony Metastases Under Radiation Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Heidelberg University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Standard indications for palliative radiation of bony metastases include pain, spinal cord compression, and impending pathologic fractures. Palliative radiation therapy serves to reduce pain, improve quality of life, and avoid complications. Tailored training of the paravertebral musculature may support radiation therapy and improve above named factors. DISPO was designed to investigate the impact of tailored physical exercise in patients with vertebral metastases as compared to manual therapy (massage etc.). The trial includes patients with painful bony metastases, patients with spinal cord compression or impending pathological fractures are excluded. The investigations are carried out in a prospective randomized controlled phase-II parallel group design.
Detailed Description
Standard indications for palliative radiation of bony metastases include pain, spinal cord compression, and impending pathologic fractures. Palliative radiation therapy serves to reduce pain, improve quality of life, and avoid complications. Tailored training of the paravertebral musculature may support radiation therapy and improve above named factors. DISPO was designed to investigate the impact of tailored physical exercise in patients with vertebral metastases as compared to manual therapy (massage etc.). The trial includes patients with painful bony metastases, patients with spinal cord compression or impending pathological fractures are excluded. The investigations are carried out in a prospective randomized controlled phase-II parallel group design. Patients are randomized to one of the following groups: patients in arm A carry out daily physical training consisting of three different isometric exercises under the guidance and supervision of a physiotherapist. Training starts day one (first radiotherapy session), 10 daily units of 30 min each are scheduled during radiotherapy. Patients are expected to continue training until 12 weeks post completion of radiotherapy at home. Patients in arm B (control group) receive 10 daily sessions of 15 min manual therapy (i.e. massage, etc) starting from day one of radiotherapy. Follow-up of the patients is scheduled at 12 weeks post completion of radiotherapy incl. CT of the spine and physical examination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vertebral Bony Metastases
Keywords
bony metastases, physical exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
patients in arm A carry out daily physical training consisting of three different isometric exercises under the guidance and supervision of a physiotherapist. Training starts day one (first radiotherapy session), 10 daily units of 30 min each are scheduled during radiotherapy. Patients are expected to continue training until 12 weeks post completion of radiotherapy at home.
Arm Title
B
Arm Type
No Intervention
Arm Description
Patients in arm B (control group) receive 10 daily sessions of 15 min manual therapy (i.e. massage, etc) starting from day one of radiotherapy.
Intervention Type
Other
Intervention Name(s)
exercise
Intervention Description
tailored isometric physical exercise
Primary Outcome Measure Information:
Title
feasibility of isometric exercise in vertebral bony metastases
Description
safety and feasibility of isometric exercise in vertebral bony metastases
Time Frame
12 weeks post completion of radiotherapy
Secondary Outcome Measure Information:
Title
progression-free survival (PFS)
Description
PFS is assessed 2 years post completion of radiotherapy
Time Frame
2 years post completion of radiotherapy
Title
fracture-free survival (FFS)
Description
FFS is assessed 2 years post completion of radiotherapy
Time Frame
2 years post completion of radiotherapy
Title
bone density
Description
bone density is assessed 12 weeks post completion of radiotherapy using follow-up CT scan of the spine
Time Frame
12 weeks post completion radiotherapy
Title
pain reduction
Description
pain is evaluated using the VAS pain scale (0-100 points) at completion and 12/ 24 weeks post completion of radiation therapy
Time Frame
end of treatment, 12 and 24 weeks post completion of radiotherapy
Title
Quality of life
Description
Quality of life is assessed using the EORTC BM22 questionnaire at 12 and 24 weeks post completion of treatment
Time Frame
12 and 24 weeks post completion of therapy
Title
Fatigue
Description
Fatigue is assessed using the EORTC FA13 questionnaire
Time Frame
12 and 24 weeks post completion of therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: solitary or multiple vertebral metastases thoracic spine lumbar spine sacrum indication for palliative radiation therapy age: 18 - 80 years Karnofsky index > 70% bisphosphonate therapy inititated Exclusion Criteria: bony metastases of cervical spine or pelvis impending fracture other serious illnesses or medical conditions: therapy-refractory unstable heart disease, congestive heart failure NYHA °III and °IV; coagulopathies Significant neurological or psychiatric condition including dementia or seizures or other serious medical condition prohibiting the patient's participation in the trial by judgement of the investigators Legal incapacity or limited legal capacity Positive serum/ urine beta-HCG/ pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juergen Debus, MD PhD
Organizational Affiliation
Heidelberg University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of Radiation Oncology, University of Heidelberg, Germany
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

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Isometric Muscle Training in Patients With Spinal Bony Metastases Under Radiation Therapy

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