Exercise Induced Muscle Damage Post Dance and Sprint Specific Exercise in Females

Exercise Induced Muscle Damage Clinical Trial

Official title:

Exercise Induced Muscle Damage Post Dance and Sprint Specific Exercise in Females

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03284450
• Other study ID #: NUMB1
• Status: Completed
• Phase: N/A
• First received: September 28, 2016
• Last updated: September 12, 2017
• Start date: April 2014
• Est. completion date: June 2014

Study information

• Verified date: September 2017
• Source: Northumbria University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is a paucity of studies investigating exercise-induced muscle damage (EIMD) in females and only one in response to dance-type exercise. This study aimed to firstly elucidate the physiological profile of EIMD following a dance-specific protocol, and second to compare the magnitude of damage to that experienced following a sport-specific protocol in physically active females.

Description:

Twenty nine female recreational dancers from a University dance team volunteered to take part in the study. A 3-day food diary and activity log completed prior to testing determined that there were no differences in physical activity levels or energy and macronutrient intakes between participants. Subjects were asked to replicate their reported diets as closely as possible throughout the testing period. A menstrual cycle questionnaire was also completed in order to determine menstrual cycle phase; all testing took place during the early/mid luteal phase.

Participants were randomly assigned to two exercise groups designed to induce EIMD; either a dance-specific protocol (DPFT) or a sport-specific repeated sprint protocol (SSRS). Participants completed the DPFT (n=15) or SSRS (n=14) and a battery of commonly used muscle damage indices were measured pre, immediately post and 24-, 48-, and 72 h post muscle damage. These were; delayed onset muscle soreness (DOMS), limb girth, countermovement jump height (CMJ), reactive strength index (RSI), maximal voluntary isometric contraction (MVC) sprint performance, and total creatine kinase (CK) activity. Participants were tested at the same time on subsequent days (± 1 h) to account for diurnal variation. Participants were asked to avoid strenuous exercise, alcohol, caffeine, nutritional supplements and any anti-inflammatory drugs or alternative treatments for the duration of the study.

Statistical software (IBM SPSS v21, IBM, USA) was used for inferential analysis and significance was accepted at the P < .05 a priori. Mauchley's test assessed the sphericity of the data and where appropriate, violations were corrected using the Greenhouse-Geisser. To explore our first objective, a one-way analysis of variance (ANOVA) with repeated measures (group, 1; time, 5) was performed on all variables in order to analyse the muscle damage response to the DPFT. For the second aim a two-way ANOVA with repeated measures (group, 2; time, 5) was used for all variables to allow for comparison of the muscle damage response between the DPFT and the SSRS. Where appropriate LSD post-hoc analysis was performed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 29
• Est. completion date: June 2014
• Est. primary completion date: June 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 25 Years

Eligibility

Inclusion Criteria:

• physically active

• at least 3 years experience in dance training

Exclusion Criteria:

• presence of any medical or physical conditions, either chronic or sustained in the last 3 months which would make participation difficult or harmful to the participant

• eg. history of cardiovascular disease and musculoskeletal disorders

Related Conditions & MeSH terms

• Exercise Induced Muscle Damage

Intervention

Other:
• DPFT
The DPFT described previously (Redding et al., 2009) involves the repetition of a 'dance phrase' representative of contemporary dance, with each phrase separated by a 2 minute rest period. For the present study the originally described test was extended; the adapted protocol involved 10 x 1 minute movement phrases, each separated by 2 minutes rest.
• SSRS
The SSRS (Howatson & Milak, 2009) involved 15 x 30 m sprints with a rapid 10 m deceleration phase, with each sprint departing every 65 seconds.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Northumbria University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in maximum voluntary contraction (MVC)	Isometric MVC of the participants' dominant knee extensors was assessed using a strain gauge.	Change from pre exercise MVC at 24 h post exercise
Secondary	Limb girths	Lower limb girths at the calf and mid-thigh of the right leg were recorded as measures of muscle swelling. Both locations were marked with permanent marker to ensure consistency on consecutive days.	pre, immediately post (0) and 24-, 48-, and 72 h post exercise
Secondary	Countermovement jump	Countermovement jump height was recorded using a light timing system.	pre, immediately post (0) and 24-, 48-, and 72 h post exercise
Secondary	Reactive strength index	Participants performed a drop jump from a 30cm height to determine reactive strength index	pre, immediately post (0) and 24-, 48-, and 72 h post exercise
Secondary	Muscle soreness	Subjective muscle soreness was measured using a 200 mm visual analogue scale from 'no soreness' to 'unbearably sore.' Participants were required to indicate on the line the level of perceived active lower limb soreness felt during a 90 degree squat.	pre, immediately post (0) and 24-, 48-, and 72 h post exercise
Secondary	30 m sprint time	Participants completed a single maximal effort 30 m sprint where sprint time was recorded. The sprint was initiated from a line 30 cm behind the start line in order to prevent false triggering of the timing gates.	pre, immediately post (0) and 24-, 48-, and 72 h post exercise
Secondary	Creatine Kinase	Blood samples were collected via venepuncture from the antecubital fossa area in to a 10 ml EDTA vacutainer. The samples were centrifuged at 3000 RCF for 15 minutes at 4 C. Plasma was extracted, and stored immediately at -80 C for later analysis. Plasma CK concentrations were determined spectrophotometrically.	pre, immediately post (0) and 24-, 48-, and 72 h post exercise