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Evaluation of Osteopathic Manipulative Treatment in the Chronic Pain and Stiffness of Chikungunya Fever

Evaluation of Osteopathic Manipulative Treatment in the chronic musculoskeletal manifestations of Chikungunya Fever: A randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-25nsk2n
Enrollment
Unknown
Registered
2022-04-13
Start date
2020-09-30
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic pain

Interventions

Analysis of pain and mobility in 40 patients of both sexes, 20 osteopathy group and 20 control group. The osteopathy group will receive 4 sessions, consisting of 7 osteopathic manipulation techniques

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Empresa Brasileira de Serviços Hospitalares
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age greater than or equal to 18 years; Diagnosis of Chikungunya Fever with positive serology chikungunya; Being in the chronic phase of the disease; Symptoms of pain and stiffness in upper limbs; Consent to participate in the study and be able to sign the consent form;

Exclusion criteria

Exclusion criteria: Patients with inflammatory joint diseases, prior to chikungunia infection; Diagnosis of diseases that compromise the functionality of the upper limbs; Presence of other chronic infectious diseases or neoplasms; Patients who had cognitive, auditory or visual deficits that prevented the application of assessment instruments; Patients who were undergoing physiotherapeutic treatment or had performed it in the last 2 months; Patients who were performing regular physical activity;

Design outcomes

Primary

MeasureTime frame
It is expected to find a difference in the mean pain intensity in relation to the initial score of at least three points, evaluated by the brief BPI pain inventory, a difference in the mean pain score in relation to the initial, indicating less pain at pressure , evaluated by Algometry and a mean difference of at least two points in the pain score in relation to the initial score, evaluated by the VAS.

Secondary

MeasureTime frame
It is expected to find a difference in the mean improvement in the functional capacity of the upper limbs using the Disabilities of the Arm, Shoulder, Hand Questionnaire, improvement in the mean score from the minimum clinically significant difference to below 33 points, a difference in means in the improvement of the functional capacity of the upper limbs with the Nine hole peg test, reduction of at least 2 seconds in the execution time.

Countries

Brazil

Contacts

Public ContactLeonora Tenório

Universidade Federal de Pernambuco

lectenorio@me.com+55(81)988794509

Outcome results

None listed

Source: REBEC (via WHO ICTRP)