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Assessment of a home exercises program with HAM/TSP individuals

Assessment of a home exercises program with HAM/TSP individuals - randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-849jyv
Enrollment
Unknown
Registered
2015-11-14
Start date
2013-12-05
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

Immune system diseases - HTLV-1 Pain HTLV-I Infections Gait Indicators of Quality of Life Posture

Interventions

The participants will be divided into three groups by random distribution table of random numbers. Group 1 will consist of 17 individuals undergoing initially a training exercise program group during
Other
E02.779.483
H02.010.625

Sponsors

Escola Bahiana de Medicina e Saúde Pública
Lead Sponsor
Escola Bahiana de Medicina e Saúde Pública
Collaborator

Eligibility

Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Individuals with diagnosis of HTLV-1 by ELISA and confirmed by Western Blot test. Have definitive diagnosis of HAM / TSP established according to the diagnostic criteria proposed by the World Health Organization. Having aged 2 to 59 years. Being able to stand. Subscribe to the free and informed consent.

Exclusion criteria

Exclusion criteria: Patients suffering from rheumatic diseases. Patients suffering from orthopedic diseases. Patients suffering from other neurological diseases. Patients with cognitive changes that compromise the understanding of the exercise program and evaluation tools used.

Design outcomes

Primary

MeasureTime frame
Increased joint angles of the trunk, hip, knee and ankle checked through the SAPO protocol, based on the statement of a variation of at least 5% in pre and post intervention. The evaluation will be held one week before and one week after the intervention.

Secondary

MeasureTime frame
Improvement in pain levels, verified by the Brief Pain Inventory, from the decrease in at least two points of the painful intensity of study participants before and after the intervention. The evaluation will be held one week before and one week after the intervention.

Countries

Brazil

Contacts

Public ContactKátia;Kátia Sá;Sá

Escola Bahiana de Medicina e Saúde Pública;Escola Bahiana de Medicina e Saúde Pública

katia.sa@gmail.com;katia.sa@gmail.com+55 (71) 3276 8200;+55 (71) 3276 8265

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Mar 3, 2026