Phototherapy in Association to Resistance Training in the Elderly: the Effect on Muscle Strength, Muscle Mass and Functional Capacity

Phototherapy has been largely used in rehabilitation programs due to its analgesic, antiinflammatory and healing effects. Lately, its effects of optimizing the results of resistance training on young individuals have been studied. However, there is a lack of studies on its effect on the elderly population. The objective of the present study is to verify the effect of Low-Level Laser Therapy (LLLT) on the results of resistance training in the elderly. The study will be a randomized doubled-blinded controlled trial. 30 elderly men with age ranging from 60 to 80 years will be included and randomized between Placebo Group (placebo LLLT + Resistance Training) and LLLT Group (active LLLT + Resistance Training). All volunteers will be submitted to a control period of four weeks before the beginning of the resistance training, which will have 12 weeks of duration. The assessments will be done at baseline, after the control period and after the training period. The training sessions will be performed twice a week and the training protocol will be performed with repetition maximum periodization. The LLLT will be applied before the training sessions on eight points of the quadriceps muscles, leading to a total of 240 Joules on each leg. The placebo LLLT will be applied on the same way, but with the equipment turned off. The assessments will include muscle architecture by ultrasonography, muscle strength by isokinetic dynamometer and 1 Repetition Maximum test of leg-extension and leg-press exercises, and functional capacity by the 6-Minute Walking Test, 30s Sit to Stand Test, Timed Up-and-Go Test and Stair Ascent Test.

Study Overview

• Status: Completed
• Conditions: Elderly Men
• Intervention / Treatment: Device: Active Low Level Laser Therapy; Behavioral: Resistance Training; Device: Placebo Low Level Laser Therapy

• Study Type: Interventional
• Enrollment (Actual): 30
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Brazil
  • Pôrto Alegre, Brazil
    • Universidade Federal do Rio Grande do Sul

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 60 years to 80 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Male

Description

Inclusion Criteria:

• Elderly men with age ranging from 60 to 80 years in condition to participate in the strength training program.

Exclusion Criteria:

• Individuals who already participate in strength training programs;
• Individuals who participated in strength training programs less than three months before the beginning of the study;
• Individuals with any kind musculoskeletal injuries in the lower limbs that impair the performance of the exercises;
• Individuals with contraindications to the performance of high intensity exercises, such as cardiovascular or neurological diseases;
• Individuals with difficulties in understanding and/or performing the exercises;
• Individuals who did not attend to at least 85% of the sessions or had 02 consecutive absences and did not recover them.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: LLLT Group; Active Low Level Laser Therapy application with a dose of 240 Joules before resistance training	Device: Active Low Level Laser Therapy; Active application of Low Level Laser Therapy with a dose of 240 Joules; Behavioral: Resistance Training; Resistance Training
Placebo Comparator: Placebo Group; Placebo Low Level Laser Therapy application before resistance training	Behavioral: Resistance Training; Resistance Training; Device: Placebo Low Level Laser Therapy; Placebo application of Low Level Laser Therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Isokinetic peak torque of quadriceps muscle	Change from baseline in isokinetic peak torque at 12 weeks

Secondary Outcome Measures

Outcome Measure	Time Frame
Leg-extension 1RM test	Change from baseline in leg-extension 1RM test at 12 weeks
Leg-press 1RM test	Change from baseline in leg-press 1RM test at 12 weeks
Muscle architecture	Change from baseline in muscle architecture at 12 weeks
Physical Function	Change from baseline in physical function at 12 weeks

Collaborators and Investigators

• Sponsor: Federal University of Health Science of Porto Alegre

Study record dates

Study Major Dates

• Study Start (Actual): March 6, 2017
• Primary Completion (Actual): December 22, 2017
• Study Completion (Actual): December 22, 2017

Study Registration Dates

• First Submitted: September 15, 2017
• First Submitted That Met QC Criteria: September 15, 2017
• First Posted (Actual): September 19, 2017

Study Record Updates

• Last Update Posted (Actual): August 1, 2018
• Last Update Submitted That Met QC Criteria: July 31, 2018
• Last Verified: July 1, 2018

More Information

Terms related to this study

• Other Study ID Numbers: 59328316.9.0000.5345

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: Yes