NCT05678400

Brief Summary

A Randomised Controlled Trial was conducted to assess increases in hamstring flexibility using two different methods, one group of participants who were stretched with PNF techniques and the other group who performed Hypopressive Abdominal Techniques (HAT). Flexibility scores of both groups were obtained and compared using pre and post measurements of a single intervention.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
19

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 2, 2023

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 10, 2023

Completed
3 months until next milestone

Study Start

First participant enrolled

March 26, 2023

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 8, 2023

Completed
22 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 30, 2023

Completed
Last Updated

January 1, 2025

Status Verified

December 1, 2024

Enrollment Period

1 month

First QC Date

January 2, 2023

Last Update Submit

December 30, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Straight leg raise test.

    The subject in supine decubitus. The patient's unscanned leg was kept stretched out on the stretcher by means of thigh straps. A digital inclinometer was placed on the other leg over the tibia before starting to lift the leg, in order to be able to quantify the degrees obtained during the test. The therapist will place one hand on the patient's heel holding the calcaneus to prevent rotation and the other on the patella to prevent the knee from flexing during the test. The examiner shall then perform a slow, progressive flexion of the hip with the knee extended, starting from 0° at rest and considering 90° when the lower limb is completely perpendicular to the examination couch. The angular value is taken as the maximum degree of flexion tolerated by the individual, the moment at which the pelvis begins to tilt in retroversion or when the examiner perceives a feeling of firm resistance.

    Baseline changes at the end of the intervention (approximately one hour).

Secondary Outcomes (1)

  • The Toe-Floor Distance test

    Baseline changes at the end of the intervention (approximately one hour).

Study Arms (2)

Hypopressive abdominal techniques

EXPERIMENTAL

All subjects were instructed by a registered physiotherapist on how to correctly perform the hypopressive abdominal techniques (HAT) in two familiarisation sessions of 45 minutes each before any action was taken. After the two sessions, all subjects who did not learn the exercise correctly were dropped from the study. The HAT training consisted of asking subjects in a standing position to perform a spinal elongation with neutral pelvis and scapular muscle activation for three normal respiratory cycles with slow and deep exhalation, and on the last breath, an expiratory apnoea with rib expansion and elevation was requested. In this session, following the guidelines described in the familiarisation sessions, two series of four dynamic HATs in standing position were performed: dynamic HATs in right tilt, dynamic HATs in left tilt, dynamic HATs in right rotation and dynamic HATs in left rotation.

Behavioral: Hypopressive abdominal techniques

Stretching of proprioceptive neuromuscular facilitation

ACTIVE COMPARATOR

The therapist straddled that leg, and raised the other leg by placing the heel on the shoulder. The therapist then flexed the participant's hip, maintaining knee extension, to the point of discomfort indicated by the patient or the therapist's perceived end of range. In this position the leg was held straight for 10 seconds and immediately afterwards the participant was asked to perform a maximum isometric contraction for 5 seconds using the therapist's shoulder as counter resistance, thus keeping the leg straight at the same point. As soon as the contraction stops, the therapist flexes the hip again until a new range limit is reached, repeating the same protocol again. The total duration is 60 seconds, consisting of 4 passive stretches of 10 seconds each and 4 isometric contractions against resistance of 5 seconds each.

Behavioral: Stretching of proprioceptive neuromuscular facilitation

Interventions

Both training protocols were carried out in a single intervention for each of the participants assigned to either the HAT or the PNF stretching group. The intervention began with the measurement of hip flexion using the EPR test, and ended with a post-intervention measurement of hip flexion to observe the effects of the treatment. All measurements, as well as the interventions for each of the patients in the two groups, were carried out by the same registered physiotherapist. In order to standardise an order of examination of the lower limbs in the EPR test, the right lower limb was assessed first, followed by the left lower limb. Likewise, the same order was standardised for stretching in the PNF group.

Hypopressive abdominal techniques

Stretching of proprioceptive neuromuscular facilitation

Stretching of proprioceptive neuromuscular facilitation

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Participants with less than 75° in the straight leg raise test.

You may not qualify if:

  • History of hamstring injury within the last year.
  • Pharmacological treatment or history of neurological, orthopaedic, growth or autoimmune disorders.
  • Training to improve flexibility in the week prior to the intervention.
  • Hypertension.
  • Pregnant women.
  • Inability to perform hypopressive abdominal techniques.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Facultade de fisioterapia

Pontevedra, 36005, Spain

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate professor in health sciences

Study Record Dates

First Submitted

January 2, 2023

First Posted

January 10, 2023

Study Start

March 26, 2023

Primary Completion

May 8, 2023

Study Completion

May 30, 2023

Last Updated

January 1, 2025

Record last verified: 2024-12

Locations