VentosaOA: Dry Cupping Therapy in Knee Osteoarthritis

Sponsor

Universidade Federal do Rio Grande do Norte (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT04331158

Collaborator

(none)

Enrollment

Location

Arms

Anticipated Duration (Months)

7.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Introduction: Knee osteoarthritis (KOA) is the biggest cause of pain and disability worldwide. As a non-pharmacological approach, ventosatherapia has been used to control pain, improve function and quality of life. However, there is a lack of high-quality scientific evidence regarding its effects on this condition. Objective: To evaluate the effects of dry cupping on pain, function and quality of life in women with KOA. Methods: This is a randomized, blinded placebo-controlled protocol. 62 women diagnosed with KOA will be recruited, based on the clinical criteria of the American College of Rheumatology, who will be randomly divided into two groups (31 per group): dry cupping and dry cupping sham.

Condition or Disease	Intervention/Treatment	Phase
Osteo Arthritis Knee Pain, Chronic Pain	Other: Dry cupping therapy	N/A

Detailed Description

The intervention will be carried out for 15 minutes, twice a week, for 6 consecutive weeks, totaling 12 sessions. Both groups will be evaluated in 4 moments: before the intervention (T0), after 3 weeks of interventions (T3), at the end of the protocol (T6) and 4 weeks after the end of the interventions (follow-up - T10). The analyzed outcomes will be: Primary - pain (numerical pain scale); Secondary - Physical function (WOMAC; tests of going up / down stairs, brisk walking in 40 m and sitting / rising from a chair in 30 s), quality of life (SF-36) and global perception of the effect

Study Design

Study Type:

Interventional

Anticipated Enrollment :

62 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Intervention Model Description:

dry cupping group and dry cupping sham groupdry cupping group and dry cupping sham group

Masking:

Double (Participant, Outcomes Assessor)

Masking Description:

To avoid any type of selection bias, the confidential allocation method will be through opaque envelopes, sealed and numbered consecutively. The randomization process will be carried out by an independent researcher who will not be involved in other study procedures. The group in which the participant will be allocated will be revealed to the researcher responsible for the consultations prior to the first intervention.

Primary Purpose:

Treatment

Official Title:

The Effects of Dry Cupping on Pain, Function and Quality of Life of Women With Knee Osteoarthritis: Protocol for a Placebo-controlled Randomized Trial

Anticipated Study Start Date :

Jul 2, 2023

Anticipated Primary Completion Date :

Dec 2, 2023

Anticipated Study Completion Date :

Mar 2, 2024

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Dry cupping group The dry cupping will be applied with a force of two suctions generating a negative pressure on the skin during the time of 15 minutes.	Other: Dry cupping therapy Dry cupping therapy application on the patient's skin
Placebo Comparator: Dry cupping sham group The dry cupping sham group will receive the same procedures as the dry cup group, with the difference that the negative pressure imposed after application will be released in a few seconds.	Other: Dry cupping therapy Dry cupping therapy application on the patient's skin

Arm

Intervention/Treatment

Experimental: Dry cupping group

The dry cupping will be applied with a force of two suctions generating a negative pressure on the skin during the time of 15 minutes.

Other: Dry cupping therapy

Dry cupping therapy application on the patient's skin

Placebo Comparator: Dry cupping sham group

The dry cupping sham group will receive the same procedures as the dry cup group, with the difference that the negative pressure imposed after application will be released in a few seconds.

Other: Dry cupping therapy

Dry cupping therapy application on the patient's skin

Outcome Measures

Primary Outcome Measures

Change from Numerical Rating Scale (NRS) [baseline, 3 ,6 and 10 weeks after.]
Subjective measure in which individuals rate their pain on an eleven-point numerical scale. Such scale will be positioned in front of the participant and will vary from 0 to 10 points, with 0 being the complete absence of pain and 10 being the worst pain imaginable by the individual

Secondary Outcome Measures

Change from Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) [baseline, 3 ,6 and 10 weeks after.]
Questionnaire translated and validated for the Portuguese language, specific for the evaluation of patients with KOA, contains 24 questions divided into three categories that assess pain, stiffness and self-reported physical function.38 The items are evaluated by a Likert scale and each question receives a score that varies from 0 to 96 points, according to the patient's response (none = 0; low = 1; moderate = 2; severe = 3; very severe = 4). The higher the score obtained, the worse the severity of pain, stiffness or physical function
Change from 30-second Chair Stand Test [baseline, 6 and 10 weeks after.]
The sit and stand test will be performed in a chair without armrests, with a height of 43 cm, with non-slip rubber under its four supports. The back of the chair will be supported by a wall to prevent oscillations during the movements of sitting and standing. The participant will sit in the middle of the chair, with an erect back, feet apart and aligned with the joints of the respective shoulders and supported on a flat and stable floor. The test will consist of getting up from the chair as many times as possible, for 30 seconds. In this way, it will be possible to assess different levels of skill, with scores ranging from 0, for those who cannot complete a single repetition, to values greater than 20 repetitions, for the most able and well-prepared individuals
Change from 8-step Stair Climb Test [baseline, 6 and 10 weeks after.]
In the test of going up and down stairs, the participant will be positioned in front of the stairs and, at the signal, must go up the indicated steps (8 steps) and go down, in the shortest time possible. The height of each step will be 20 cm and it will be a staircase with a handrail, in a lighted environment, free of traffic and external distractions. A pre-test will be carried out to identify the need for security measures. The final score will be calculated based on the time the participant performed the procedure and compared with normative values available for the test.
Change from 40m Fast Paced Walk Test [baseline, 6 and 10 weeks after.]
The 40 meter fast walk test will be performed on 4 circuits of 10 meters (marked by ribbons and bounded by cones), in which the participant will be guided to walk the 10 meters, go around the cone and travel the next 10 meters again, successively, until the total distance of 40 meters is completed. The time will be timed only between the markings (start and end). The final score will be calculated based on the time the participant will perform the procedure and compared with normative values for healthy adults.
Change from Short-Form 36 quality of life [baseline, 6 and 10 weeks after.]
The instrument consists of 36 questions and assesses eight different domains that influence quality of life, considering the individual's perception of aspects of his health in the past weeks. Each item has a group of responses distributed on a graduated Likert scale, with the following dimensions: physical function, physical aspect, pain, general health, vitality, social function, emotional aspect and mental health. Your total score ranges from 0 to 100, where the higher the value, the better the quality of life.

Eligibility Criteria

Criteria

Ages Eligible for Study:

50 Years to 75 Years

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

Inclusion Criteria:

Diagnosed with KOA based on ACR clinical criteria;
Knee pain intensity between 3 and 8, according to the Numerical Pain Scale (END);
BMI less than 35 kg / m2.

Exclusion Criteria:

Having undergone physical therapy treatment for the knee in the 3 months prior to the project;
Be engaged in> 45 minutes / week in accumulated physical activity of at least moderate intensity;
To have been submitted to the application and / or intervention with the wind therapy previously.
Have used corticosteroid infiltration in the knee in the last 6 months;
Present any medical restrictions that make it impossible for them to participate in the proposed assessments and interventions (cardiorespiratory, neurological and / or musculoskeletal changes);
Presenting a diagnosis of fibromyalgia, rheumatoid arthritis or some systemic inflammatory arthritis;
Presenting a ligament or meniscal injury diagnosed clinically or with a positive result in the Apley tests or anterior / posterior drawer;
Have had previous surgery on the ankle, knee or hip;
Present a clinical diagnosis of some dementia or inability to answer the questionnaires related to the study;
Present any contraindications for the use of ventosatherapia (skin lesion in the region where it will be applied, cancer, kidney failure, liver and heart failure, pacemaker, pregnancy);
Having uncontrolled diabetes and hypertension;
Have a trip scheduled for the two months following inclusion in the survey.