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High-Intensity-Interval-Training in Geriatric Rehabilitation - A Feasibility Study

K

Klinik Valens

Status

Unknown

Conditions

Post-Operative Condition
Rehabilitation
Oncology
Deconditioning After Acute Hospital

Treatments

Other: High Intensity Interval Training

Study type

Interventional

Funder types

Other

Identifiers

NCT04025385
KLV-BA-2019-1

Details and patient eligibility

About

Study with Patients (40-60 participants) above the age of 65. There will be a comparison of regular training on ergometer (10 trainings within 2 weeks, 40 min each) to high intensity interval training on ergometer (6 trainings within 2 weeks, 25 min each). At the beginning and at the end will be a spiroergometer to measure the individual limits and vO2max, which will be compared amongst the two groups. To receive a subjective feedback, there will be a series of questionnaires at the beginning, after one week and at the end. The goal of this study is to get more information about whether a HII-Training is feasible with elderly patients and whether they can profit form it.

Enrollment

60 estimated patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • cardiopulmonal resilient
  • able to sit on a ergometer
  • knowledge of German written and spoken

Exclusion criteria

  • Severe cardiopulmonary restriction (LVEF <30%, conduction abnormalities from AV block IIb or higher)
  • Absolute cardiopulmonary contraindications (acute coronary syndrome, unstable AP -> not capable of rehabilitation), uncompensated heart failure (dyspnea at rest, orthopnea, severe edema)
  • No ischemic events (cardiac, cerebral, peripheral) within the last 3 months
  • Severe pneumatological underlying disease: COPD GOLD 3 and higher or status after exacerbation within the last 2 weeks, Asthma grade 4
  • Dyalisis reliant
  • Severe psychiatric disorder (severe psychosis, severe depression)
  • Distinct dementia

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Control Group
No Intervention group
Description:
Patients will participate in regular training units
HIIT Group
Active Comparator group
Description:
Patients will participate in high intensity interval training
Treatment:
Other: High Intensity Interval Training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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