NCT03350880

Brief Summary

Comparison of therapeutic intervention to gain range of motion at the hip joint within therapeutic in water and on land. Stretching is a therapeutic maneuver used to increase the length of shortened soft tissue structures and thereby gain range of motion; for that, innumerable procedures within Physiotherapy use it for the benefit of patients. The work in question is justified by the need to seek the means that can promote a better performance in the application of the stretching procedure, called Proprioceptive Neuromuscular Facilitation, in a universe of pre-selected volunteers. It is a relevant and feasible study, hoping that its results may benefit future patients, with better results and faster responses. What is the medium that leads to better results in a program using the proprioceptive neuromuscular facilitation technique? Hypotheses: a - Probably the heated aquatic environment, in a range of 32 ° to 36 ° C, will promote a better result, since the heat increases the collagen's distensibility. b - Perhaps the heat, by increasing the excitability threshold of nerve fibers, triggers the "protective reflex" later, which may promote a more vigorous elongation without the protective response. c - Possibly the relaxation promoted in the aquatic environment, could influence the gains obtained in the swimming pool.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2018

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

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

November 18, 2017

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 22, 2017

Completed
1 month until next milestone

Study Start

First participant enrolled

January 1, 2018

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 28, 2018

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2018

Completed
Last Updated

July 29, 2022

Status Verified

July 1, 2022

Enrollment Period

8 months

First QC Date

November 18, 2017

Last Update Submit

July 27, 2022

Conditions

Keywords

PassiveStretchingWaterProprioceptive Neuromuscular Facilitation (PNF)

Outcome Measures

Primary Outcomes (1)

  • range of motion

    range of motion by goniometer

    six weeks

Secondary Outcomes (1)

  • sit and reach test

    six weeks

Study Arms (2)

PNF in Water - PNFW

EXPERIMENTAL

Flexibility training was carried out over a period of six weeks, with two sessions per week, totaling 12 sessions.

Other: Flexibility training

PNF on Land - PNFL

ACTIVE COMPARATOR

Flexibility training was carried out over a period of six weeks, with two sessions per week, totaling 12 sessions.

Other: Flexibility training

Interventions

Flexibility training was carried out over a period of six weeks, with two sessions per week, totaling 12 sessions.

Also known as: streching training
PNF in Water - PNFWPNF on Land - PNFL

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • age between 18 and 60 years;
  • sedentary and who did not perform physiotherapy and physical activity in the last three months;
  • clinical and cognitive conditions for swimming pool activities and aerobic exercise; who have not undergone highly complex surgical procedures in the last six months;
  • to be able of walking without help equipment and without musculoskeletal or skeletal diseases;
  • without contraindications to the practice of exercises; such as: urinary and / or fecal incontinence and dermatological diseases;
  • below obesity II with BMI \<40.

You may not qualify if:

  • if they have up to three consecutive fouls during the hydrogymnastics period;
  • if they present any adverse effects, such as: allergy or any dermatitis;
  • unable to continue the study due to change of address or hospitalization.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Physical Education College

Petrolina, Pernambuco, 56304917, Brazil

Location

Related Publications (1)

  • Ribeiro, Hálisson Alves, et al.

    RESULT

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized Clinical Trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Master

Study Record Dates

First Submitted

November 18, 2017

First Posted

November 22, 2017

Study Start

January 1, 2018

Primary Completion

August 28, 2018

Study Completion

November 1, 2018

Last Updated

July 29, 2022

Record last verified: 2022-07

Data Sharing

IPD Sharing
Will share

Papers and abstract congress

Shared Documents
CSR
Time Frame
one year
Access Criteria
age between 18 and 60 years; sedentary and who did not perform physiotherapy and physical activity in the last three months; clinical and cognitive conditions for swimming pool activities and aerobic exercise; who have not undergone highly complex surgical procedures in the last six months; to be able of walking without help equipment and without musculoskeletal or skeletal diseases; without contraindications to the practice of exercises; such as: urinary and / or fecal incontinence and dermatological diseases; below obesity II with BMI \<40.

Available IPD Datasets

Clinical Study Report Access

Locations