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Differentiated Resistance Training of the Paravertebral Muscles in Patients With Unstable Spinal Bone Metastasis Under Concomitant Radiotherapy

Differentiated Resistance Training of the Paravertebral Muscles in Patients With Unstable Spinal Bone Metastasis Under Concomitant Radiotherapy

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02847754
Acronym
DISPO-2
Enrollment
60
Registered
2016-07-28
Start date
2016-08-31
Completion date
2020-01-31
Last updated
2016-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vertebral Bony Metastases

Keywords

bony metastases, physical exercise

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-2 was designed to investigate the impact of tailored physical exercise in patients with unstable vertebral metastases as compared to manual therapy (massage etc.). The trial includes patients with painful unstable 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-2 was designed to investigate the impact of tailored physical exercise in patients with unstable vertebral metastases as compared to manual therapy (progressive muscle relaxation). 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 four 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 progressive muscle relaxation 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.

Interventions

Exercises in the all-fours position Exercises in the swimming Position Exercises in the forearm support Position Exercises with elastic rubber band

Sponsors

Heidelberg University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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 initiated

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

Design outcomes

Primary

MeasureTime frameDescription
feasibility of isometric exercise in unstable vertebral bony metastases12 weeks post completion of radiotherapycompletion of all isometric exercises until 12 weeks post RT

Secondary

MeasureTime frameDescription
fracture-free survival (FFS)2 years post completion of radiotherapyFFS is assessed 2 years post completion of radiotherapy
bone density12 weeks post completion radiotherapybone density is assessed 12 weeks post completion of radiotherapy using follow-up CT scan of the spine
progression-free survival (PFS)2 years post completion of radiotherapyPFS is assessed 2 years post completion of radiotherapy
Quality of life12 and 24 weeks post completion of therapyQuality of life is assessed using the EORTC BM22 questionnaire at 12 and 24 weeks post completion of treatment
Fatigue12 and 24 weeks post completion of therapyFatigue is assessed using the EORTC FA13 questionnaire
pain reductionImmediately after completion of radiotherapy, 12 and 24 weeks post completion of radiotherapypain is evaluated using the VAS pain scale (0-100 points) at completion and 12/ 24 weeks post completion of radiation

Countries

Germany

Contacts

Primary ContactHarald Rief, MD, PhD
harald.rief@med.uni-heidelberg.de
Backup ContactJürgen Debus, MD, PhD
juergen.debus@med.uni-heidelberg.de

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026