Healthy Subjects Clinical Trial
Official title:
Randomized Controlled Trial of Two Combinations of Strength and Sensorimotor Training: Effects on Strength, Power and Balance
AIM:
Strengthening and sensorimotor training (e.g with the aim to improve balance) are widely
used in rehabilitation. There is little knowledge about the best ways to combine
strengthening and sensorimotor training. Therefore, the investigators want to evaluate two
types of combinations in healthy participants.
Interventions:
- Group A: 1.) warm-up; 2.) sensorimotor training; 3.) strength training (nine sessions
in four weeks)
- Group B: 1.) warm-up; 2.) one strengthening exercise, followed by a sensorimotor
exercise, alternating (nine sessions in four weeks)
Tests (Before first training and after four weeks):
- isokinetic test of knee extensors and flexors (60°/s; 120°/s; 180°/s; 240°/s.)
- squat jumps and countermovement jumps
- static balance test on an unstable underground (measured with accelerometer)
- dynamic balance: star excursion balance test, (a) on stable ground, (b) on unstable
ground. Balance tests will be performed (c) in recovered state and (d) fatigue (i.e.
after a fatiguing exercise).
Hypotheses
1. Group B (alternating sensorimotor and strength exercises) will improve more in the
balance tests than Group A (sensorimotor first, strength afterwards).
2. Group B will improve more in the countermovement jump than Group A.
3. There will be no differences in the improvements in the strength, power and squat jump
tests between the two groups.
Status | Completed |
Enrollment | 30 |
Est. completion date | December 2008 |
Est. primary completion date | December 2008 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Able to perform strength and sensorimotor training - At least 18 years old Exclusion Criteria: - Injury that does not allow training and testing - Illness that does not allow training and testing - Pregnancy - Pain during exercising |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Switzerland | School of Physiotherapy, University of Applied Sciences Western Switzerland, Valais | Leukerbad | Valais |
Lead Sponsor | Collaborator |
---|---|
University of Applied Sciences of Western Switzerland |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Dynamic Balance measured with the Star Excursion Balance Test | From baseline to four weeks | No | |
Secondary | Change in height with counter-movement jump | From baseline to four weeks | No | |
Secondary | Change in height with squat jump | From baseline to four weeks | No | |
Secondary | Change in force development (Nm) in knee extensors and knee flexors | From baseline to four weeks | No | |
Secondary | Change in Power knee extensors and knee flexors | From baseline to four weeks | No | |
Secondary | Change in Static Balance (single leg stance on unstable ground) | From baseline to four weeks | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05483998 -
A Study to Evaluate Single and Multiple Doses of TLC-2716 in Healthy Participants
|
Phase 1 | |
Recruiting |
NCT02417714 -
Prospective Evaluation of Next Generation CT Reconstruction (NextGenIR)
|
||
Recruiting |
NCT02235012 -
Cognitive Biases Under Ketamine
|
N/A | |
Completed |
NCT05088343 -
Effect of Hetrombopag on the Pharmacokinetics of Rosuvastatin in Healthy Subjects
|
Phase 1 | |
Completed |
NCT04418973 -
Analysis of Breath Volatile Organic Compounds After Dyspnea Induced in the Healthy Subject.
|
N/A | |
Not yet recruiting |
NCT06248801 -
Vildagliptin and Metformin Tablets 50/1000 mg Relative to GALVUS MET (50mg/1000 mg) Tablets
|
Phase 1 | |
Terminated |
NCT04068259 -
Single Ascending Dose Study of PBI-4547 in Healthy Subjects
|
Phase 1 | |
Completed |
NCT03279302 -
Trial to Evaluate the PK Profile of Glepaglutide (ZP1848) After a Single IV and After Multiple SC Injections in Healthy Subjects
|
Phase 1 | |
Not yet recruiting |
NCT06233162 -
Febuxostat 80 mg Tablets Relative to Feburic® 80 mg Tablets
|
Phase 1 | |
Recruiting |
NCT04159844 -
Evaluation of the Stiffness and Pressure Applied on the Lower Leg by a New Compression Bandage on Healthy Subjects
|
N/A | |
Completed |
NCT06137911 -
Evaluation of Safety, Tolerability & Pharmacokinetics of JYP0061 in Healthy Adults.
|
Phase 1 | |
Completed |
NCT04849286 -
Measurement of HTL0016878 in Cerebrospinal Fluid
|
Phase 1 | |
Not yet recruiting |
NCT06233227 -
Dutasteride Soft Capsule 0.5 mg Relative to Avodart 0.5 mg Soft Capsule
|
Phase 1 | |
Completed |
NCT04096157 -
A Study to Assess Isavuconazole Following a Single Dose of Isavuconazonium Sulfate Intravenous Solution Via Nasogastric (NG) Tube Compared to a Single Dose of Oral Capsules Under Fasting Conditions in Healthy Participants
|
Phase 1 | |
Completed |
NCT01200368 -
Trial Evaluating a 13-valent Pneumococcal Conjugate Vaccine Given With Diphtheria, Tetanus, and Acellular Pertussis Vaccine (DTaP) in Healthy Japanese Infants
|
Phase 3 | |
Recruiting |
NCT05805033 -
Peri-Implant Soft Tissue Integration in Humans: Influence of Material
|
N/A | |
Completed |
NCT04027803 -
Comparative Study of Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of Single Intravenous Doses of BCD-148 and Soliris®
|
Phase 1 | |
Recruiting |
NCT03467880 -
Multicenter Study of Impulse Oscillometry in Chinese
|
N/A | |
Completed |
NCT02903095 -
Single Ascending Dose Study of TD-1439 in Healthy Subjects
|
Phase 1 | |
Active, not recruiting |
NCT02341508 -
A Phase 1a, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate Lpathomab in Healthy Volunteers
|
Phase 1 |