NCT02702219

Brief Summary

Mobility training in the form of stretching and flexibility training of our skeletal muscle is a common exercise. However, the evidence are scare and there are only a few studies comparing the effect of prolonged static stretching (\> 90 sec) and dynamic flexibility training as to which of these methods has the best length-enhancing effect over time. Further, in clinical practice concerning low back pain, the possibility of a thigh hamstrings muscles to affect movement control of the spine is often mentioned, a link not fully explored in a controlled condition. The purpose of this study is to compare the effect of eight weeks of dynamic flexibility training versus prolonged static stretching on mobility in the hamstring muscles in adults with reduced mobility in the muscles at the back of the thigh. The aim is also to compare the sustained effect of flexibility training between the two groups, eight weeks after completion of the intervention. Furthermore, the aim is to explore how different forms of flexibility training affects movement patterns of the lumbar spine in adult persons with reduced mobility in the hamstrings.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2016

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 26, 2016

Completed
4 days until next milestone

Study Start

First participant enrolled

March 1, 2016

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 8, 2016

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
Last Updated

September 19, 2022

Status Verified

September 1, 2022

Enrollment Period

6 months

First QC Date

February 26, 2016

Last Update Submit

September 15, 2022

Conditions

Outcome Measures

Primary Outcomes (2)

  • Change of Range of motion of hip flexion

    Hip flexion is performed in a standardised procedure and is measured in degrees.

    Change from Baseline to after intervention (8 weeks), Change from Baseline to follow-up at 16 weeks

  • Change of Fingertip to floor distance

    Distance from fingertip to floor test is performed in a standardised manner and is measured in centimeters

    Change from Baseline to after intervention (8 weeks), Change from Baseline to follow-up at 16 weeks

Secondary Outcomes (2)

  • Change in Waiters bow

    Change from Baseline to after intervention (8 weeks), Change from Baseline to follow-up at 16 weeks

  • Change in Sitting bilateral knee extension

    Change from Baseline to after intervention (8 weeks), Change from Baseline to follow-up at 16 weeks

Study Arms (2)

Dynamic streching

EXPERIMENTAL

Mobility training of the hamstrings muscles to be performed every day

Behavioral: Mobility of the hamstrings muscles

Static stretching

ACTIVE COMPARATOR

Static stretching of the hamstrings muscles to be performed every day

Behavioral: Mobility of the hamstrings muscles

Interventions

Dynamic strechingStatic stretching

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Restricted hip flexion \< 80 degress due to thight hamstrings muscles

You may not qualify if:

  • discomfort or illness from musculoskeletal system which significantly affects the person in his/her everyday life
  • previous injury (within 12 weeks) in the hamstring muscle prior to study entry
  • known RA diagnosis
  • known neurological disease
  • medication affecting the musculskeletal system

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 26, 2016

First Posted

March 8, 2016

Study Start

March 1, 2016

Primary Completion

September 1, 2016

Study Completion

September 1, 2016

Last Updated

September 19, 2022

Record last verified: 2022-09

Data Sharing

IPD Sharing
Will not share