Comparison Between Two Physical Therapy Treatments in Patients With Nonspecific Chronic Neck Pain

Non-specific Chronic Neck Pain Clinical Trial

Official title:

Comparison Between Two Physical Therapy Treatments in Patients With Nonspecific Chronic Neck Pain

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04695730
• Other study ID #: 679/2020/Sper/AOUBo
• Status: Completed
• Phase: N/A
• Start date: February 9, 2021
• Est. completion date: August 31, 2022

Study information

• Verified date: September 2022
• Source: University of Bologna
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Introduction: Non-specific chronic neck pain is a very prevalent condition in the population ranging from 45% to 54%. Several conservative treatments have been shown to be effective and are currently used in clinical practice. However, among the physical therapy ones, no study evaluated the effectiveness of Pompage techniques in addition to an active treatment.

This protocol describes a controlled, randomized trial that aims to assess the effectiveness of two physical therapy treatments in patients with chronic non-specific neck pain.

Methods: Seventy subjects with chronic nonspecific neck pain from 18 to 80 years will be recruited according to the inclusion criteria.

Afterwards they will be randomized to one of the 2 groups: group 1 (G1) will undergo an active intervention and group 2 (G2) will receive the same active intervention plus manual technique. Active intervention, according to the current guidelines on non-specific neck pain, will be a treatment including both pain education and home exercises; manual technique will be the so-called "Pompage" technique.

A booster session will be planned for both groups after 4 weeks from the beginning of the trial, to reinforce the patients adherence to the self-treatment.

The patients will be evaluated before the treatments (baseline, T0), after 8 weeks from the beginning of the treatments (T1), and 6 months after the end of the treatments (T2).

The primary outcome will be pain perception, which will be assessed using a Visual Analogue Scale (VAS).

The secondary outcomes will be: kinesiophobia (measured with the Tampa Scale of Kinesiophobia

• TSK), physical function (measured with the Neck Disability Index - NDI), active cervical range of motion - ROM (measured with the "CROM Deluxe" device), patient satisfaction for treatment (measured with the Physical Therapy Satisfaction Questionnaire - PTPSQI(15)), and subjective perception of improvement (measured with the Global Perceived Effect - GPE).

Adverse effects will be registered. Discussion: Considering that there is no consensus on the use of Pompage techniques in addition to an active treatment in individuals with nonspecific chronic neck pain, our protocol will be the basis for the use of these techniques by health professionals and for new studies to be performed.

Description:

PROTOCOL OF INTERVENTIONS

The intervention of group 1 (G1) is based on education and selective strengthening exercises for cervical muscles, and involves a protocol that must be performed by the patient for 8 weeks. Halfway through the course (at the end of the fourth week) the physical therapist will carry out a reinforcement session, to monitor the clinical situation, motivate the patient and resolve any doubts (booster session).

In group 2 (G2) the "Pompage" treatment will be added to this intervention.

HOME EXERCISES: CONTENTS

In the first session supervised by a physical therapist, lasting 30 minutes, the patient will be taught all the home exercises that he/she will have to perform and will be given:

1. a hard copy with the exercise reminder;

2. a diary for recording the daily execution of the exercises. The patients will be instructed to perform the exercises on a daily basis, without feeling pain. These exercises focus on strengthening the deep muscles of the neck; cranio-cervical flexor muscles and cervical extensors.

PAIN EDUCATION: CONTENTS

The educational intervention will take place verbally in a 30-minute session (explanation by the physical therapist), and will be supported by images, diagrams and summaries.

During this intervention, the patient will be provided with information on chronic non-specific cervical pain and on "pain neuroscience education". The education session will focus on explaining the mechanisms through which the body perceives and interprets pain. The aim is to make the patient aware that experiencing pain does not necessarily mean that there is a damage on a part of the body. During this educational session, the physical therapist will try to encourage the patient to ask questions.

At the end of this session, the patient will be given an information booklet on pain, with references to the themes just explored. This booklet provides further examples and ideas for elaborating and fixing the concepts learned during the session supervised by the physical therapist.

MANUAL THERAPY: CONTENTS

The treatment of group 2 (G2) combines the previous treatments with eight 30-minutes sessions of passive manual therapy, using the "Pompage" technique, carried out according to the indications shown in the monograph: "Zanella F, Vanti C. Pompage technique. The myofascial release. Piccin, Padua, 2015." The "Pompage" technique includes gradual and progressive soft tissue and fascia mobilization procedures, with the aim to obtain the myofascial release. This procedure is performed without provoking pain or forcing movements beyond the passive physiological range of motion. It consists of an alternation of rhythmic pressure and decompression, located at cervical joints and muscles (e.g. Trapezius Superior, Levator scapulae, Scalenus, Sterno-Cleido-Occipito-Mastoideus, etc.).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: August 31, 2022
• Est. primary completion date: June 17, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Female and male subjects aged between 18 and 80 years with non-specific neck pain lasting for more than 3 months.

• Informed consent

Exclusion Criteria:

• Subjects with acute or subacute neck pain;

• Subjects with specific etiology for neck pain (e.g. trauma, herniated disc, vertebral deformities, fractures);

• Subjects with central or peripheral neurological signs;

• Individuals with systemic diseases, neuromuscular diseases, rheumatic diseases, cognitive deficit, tumors;

• Subjects who underwent surgery within 6 months preceding enrollment;

• Subjects who underwent physical therapy treatment within 6 months preceding enrollment.

Related Conditions & MeSH terms

• Neck Pain
• Non-specific Chronic Neck Pain

Intervention

Other:
• Active physical therapy (including both pain education and home exercises)
One session (60 minutes). In this session, a physical therapist will explain and demonstrate the exercises to perform individually at home. Exercises will be performed daily. In addition, an education session will be provided, concerning pain mechanisms and management. To support patients during the treatment, a booklet will be created. One booster session (30minutes) will be planned after 4 weeks. Patients will follow the active treatment for 8 weeks.
• Active physical therapy plus manual therapy
Participants in the Group 2 will receive active intervention plus 8 "Pompage" technique sessions (1 session/week). In these sessions (30 minutes each), "Pompage" technique will be performed by a physical therapist.

Locations

Country	Name	City	State
Italy	University of Bologna - Italy	Bologna

Sponsors (1)

Lead Sponsor	Collaborator
University of Bologna

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in neck pain	Visual Analogue Scale (VAS). VAS is a unidimensional measure of pain intensity. The scale is most commonly anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 100 [100-mm scale]).	At baseline, 8 weeks, and 6 months.
Secondary	Changes in neck disability	Italian version of Neck Disability Index (NDI) The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage and includes a total of 10 items.; Score: /50 Transform to percentage score x 100 = %points	At baseline, 8 weeks, and 6 months.
Secondary	Changes in Kinesiophobia/Fear of movement	Italian version of Tampa Scale of Kinesiophobia (TSK). Tampa Scale of Kinesiophobia (TSK), provides a measure of fear of movement or injury. The Italian version comprises 13 item divided in two subscales: TSK 1 - Activity Avoidance, and TSK 2-Harm.; TSK 1 - Activity Avoidance (item 1, 2, 10, 14, 15, 17):___/24; TSK 2 - Harm (item 3, 5, 6, 7, 9, 11, 13):___/28 The maximum score is 52. An higher score is related to an higher level of fear.	At baseline, 8 weeks, and 6 months.
Secondary	Changes in Active Cervical Range of Motion	"CROM Deluxe" device	At baseline, 8 weeks, and 6 months.
Secondary	Assessment of the satisfaction for physical therapy	Italian version of Physical Therapy Satisfaction Questionnaire - (PTPSQ-I(15) PTPSQ-I(15) consists of 15 items; for each item the score ranges from 1 to 5. An higher score is related to an higher level of satisfaction.	At 8 weeks and 6 months.
Secondary	Assessment of the global perception of improvement on a 7-points Likert Scale	Global Perceived Effect (GPE) questionnaire. The GPE is composed of 1 question on a 7-point Likert-type scale evaluating the subjective self-reported improvement or deterioration after the intervention. GPE is widely used in the physical therapy literature. On the basis of GPE score, patients will be dicotomized into "improved" (a score of 1-3 on the GPE) and "worsened" (a score of 5-7 on the GPE).	At 8 weeks and 6 months.