Alicia Masip
Alcalá de Henares, Madrid, 28801, Spain
NCT Number: NCT04981574
Objective:
To compare the effectiveness of thoracic thrust manipulation, together with massages techniques and stretching, between people with neck pain versus people with low back pain.
Methods:
The research will be performed from August 2021 to October 2021 at the University of Alcala de Henares. (Madrid)
A minimum of forty-six (46) volunteers will participate in this research, and they will be divided in two groups of twenty-three (23). One group will be formed by candidates suffering from neck pain (group A) and the other one by candidate with low back pain (group B).
Both groups will receive the same treatment and specific stretching exercises as applicable in accordance to the pain area, e.g.: group A will get the massage and the stretching exercises more suitable for the neck pain and group B the same but for the low back pain. Nevertheless both groups will receive the same technical thrust manipulation in thoracic area.
All these treatments will be applied of the volunteers at the University of Alcalá.
The treatment includes the following activities:
1. Twenty (20) minutes massage in the pain area, as applicable. 2. Technical thrust manipulation in thoracic area. 3. Ten (10) minutes stretching in accordance to the pain area treated. The stretching shall be repeated twice a week by each volunteer.
A total of six (6) sessions will be carried out during six (6) weeks, one session per week.
Pain, disability, kinesiophobia, HRQoL will be assessed as follow:
1. Before first session. (In this evaluation will be also analyzed demographic variables i.e.: height, weight, age, gender, academic level, smoker/no smoker) 2. Between third and fourth session. 3. After sixth session. 4. Four weeks after sixth session.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Not applicable
Alcalá de Henares, Madrid, 28801, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
using a Visual Analogue Scale (VAS) from 0 to 10
Time frame: Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
Using the Neck Disability Index (NID) Questionnaire
Time frame: Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
Using the SF-12 Quality of Life Questionnaire
Time frame: Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
Using the fear avoidance beliefs (FAB) questionnaire
Time frame: Baseline, 3 weeks, 6 weeks, and 10 weeks after intervention commencement
Using the Oswestry Disability Index (ODI) Questionnaire
University of Jaén
Other
Comparison of the Effectiveness of the Thoracic Thrust Manipulation in People With Neck or Low Back Pain
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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