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

Rehabilitation Clinical Trial

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04025385
• Other study ID #: KLV-BA-2019-1
• Status: Active, not recruiting
• Phase: N/A
• Start date: July 30, 2019
• Est. completion date: December 15, 2021

Study information

• Verified date: March 2021
• Source: Klinik Valens
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 60
• Est. completion date: December 15, 2021
• Est. primary completion date: September 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Deconditioning After Acute Hospital
• Neoplasms
• Oncology
• Post-Operative Condition
• Rehabilitation

Intervention

Other:
• High Intensity Interval Training
Training for 25 min with four 1 minute intervals when participants exercise up to 80% of their individual limits.

Locations

Country	Name	City	State
Switzerland	Rehazentrum Walenstadtberg	Walenstadtberg

Sponsors (1)

Lead Sponsor	Collaborator
Klinik Valens

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Will there be a change in outcome of individuals vO2max?	Measurement of vO2max with spiroergometer at the beginning and end	2 Weeks
Primary	Is a High intensity interval training feasible with elderly patients in rehabilitation?	Questionnaire (Clinic-intern questionnaire) amongst the involved personal	1 Day
Secondary	Will there be a change in subjective quality of life?	Questionnaires (PROMIS-10, EQ-5D) amongst the participants	2.5 Weeks