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Completed

NCT Number: NCT04345211

Manual Therapy, Thera-band Exercise and Walking

Worldwide, the number of older adults is expected to more than double by 2050 and more than triple by 2100, with most of the increase in developing countries. This situation has become a challenge to health professions such as physical therapy, since aging involves a gradual reduction in the capacity to adapt and an increase in vulnerability to health issues such as chronic non-communicable diseases and musculoskeletal disorders. The respiratory system, as the rest of the body, is exposed to both physiological aging and disease. According to the World Health Organization , respiratory diseases such as trachea, bronchi, or lung cancer, lower respiratory tract infections, or chronic obstructive pulmonary disease are found in the third, fifth, and sixth cause of death, respectively, among the top ten.

Therefore, bronchopulmonary and thoracic pathology constitutes an important problem for Public Health, both due to the high number of affected subjects and to their potential severity For this reason, the recommendations of the European, North American and national societies, highlight, among other aspects, the importance of the prevention of these diseases. They also insist on the need to maintain the integrity of the thoraco-abdominal anatomical elements and preventive treatment in those at risk, before symptoms appear. These recommendations together with the change of perspective that is being taken into account when treating aging have led to the fact that in the last decade more research has been started on the respiratory system in older people without respiratory problems.

The aim of this trial is to investigate whether manual therapy, elastic band exercise or walking can mitigate the effects of age-related changes in lung function in adults over 60 years old. Also whether there is a difference in effect between the different forms of therapy.

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Key information

Conditions

Age range

60 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Gemma Espí

Valencia, 46010, Spain

About this study

Study design A 4-week program will be implemented with sessions 2 days a week, 45-60 minutes per session. It would be convenient for each group to have 30 participants each. Group1: walking group. 40 minutes walking with supervision of the physiotherapist. 2 times per week.; Group 2: walking (40 minutes) plus self-administered thorax manual therapy (20 minutes). It will be applied in group and supervised by a physiotherapist. 2 times per week.; Group 3: walking (40 minutes) plus thorax exercises with elastic-band (20 minutes). It will be applied in group and supervised by a physiotherapist. 2 times per week.;Group 4: control group will do usual life and assessments as the rest of the groups.

Oucome measures Pulmonary function: pulmonary function evaluation via forced spirometry dynamic lung volumes (forced vital capacity, FVC; forced expired volume at 1 second, FEV1). Chest wall expansion: A measuring tape is used to measure chest expansion in centimetres (cm) at two levels of the rib cage: upper chest expansion and lower chest. Exercise tolerance: 6 Six Minute Walk Test. Smoking Index. The smoking index is a unit for measuring cigarettes consumption over a long period. Musculoskeletal Pain: visual analog scale. The pain VAS is a unidimensional measure of pain intensity, which has been widely used in diverse adult populations. Perception of change after treatment: Patient Global Impression of Improvement. Quality of life. Trigger points pain: by algometer. Change in thorax position: Distance between acromion-bed. Functional capacity: Sit-to-stand. Frailty: FRAIL Questionnaire. Motivation and self-efficacy: Participation motives are measured with the Exercise Motivation Index.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults between 60-85 years old.
  • Male and female
  • No history of respiratory or cardiac disease
  • Currently non-smoking (> 6 months)
  • Willingness to provide written consent
  • Willingness to participate in and comply with study requirements

Exclusion criteria

  • Adults over 85 years old.
  • History of respiratory pathology.
  • History of cardiac pathology.
  • Inability to walk unaided and unassisted
  • Acute pain on thoracic joint range of motion testing
  • Contra-indicated for thoracic mobilisation and/or manipulation (physical screening examination)
  • Inability to provide informed consent, e.g. people with a cognitive impairment, intellectual disability or mental illness

Treatment and study plan

Group1, walking group

Other

The walking group includes a weekly walking goal of 75 minutes.

Group 2, Walking plus manual therapy

Other

Walking plus self-administered thorax manual therapy

Group 3; Walking plus exercises with Theraband

Other

Walking plus thorax exercises with Theraband

Primary outcomes

  1. Pulmonary function

    Time frame: 4-8 week

    pulmonary function evaluation via forced spirometry dynamic lung volumes (forced vital capacity, FVC; forced expired volume at 1 second, FEV1).

Secondary outcomes

  1. Chest expansion

    Time frame: 4-8 week

    A measuring tape is used to measure chest expansion in centimetres (cm) at two levels of the rib cage: upper chest expansion and lower chest.

  2. Exercise tolerance

    Time frame: 4-8 week

    6 Six Minute Walk Test (6MWT). The object of this test is to walk as far as possible for 6 minutes. The patient will walk back and forth around the cones in a hallway and is permitted to slow down, to stop, and to rest as necessary (but resume walking as soon as able).

  3. Smoking

    Time frame: 4-8 week

    The smoking index is a unit for measuring cigarettes consumption over a long period and was calculated using the following formula:

    Smoking index = Cigarettes Smoked per Day (CPD)× years of tobacco use.

    Smoking index categories were non-smoker, <400, 400-799, and ≥800. The CPD was estimated for current and former smokers. We defined heavy smoking as ≥20 CPD and mild smoking as <20 CPD.

    The smoking index is a unit for measuring cigarettes consumption over a long period and was calculated using the following formula:

    Smoking index = Cigarettes Smoked per Day (CPD)× years of tobacco use.

    Smoking index categories were non-smoker, <400, 400-799, and ≥800. The CPD was estimated for current and former smokers. We defined heavy smoking as ≥20 CPD and mild smoking as <20 CPD.

  4. Musculoskeletal Pain

    Time frame: 4-8 week

    visual analog scale (VAS). The pain VAS is a unidimensional measure of pain intensity, which has been widely used in diverse adult populations.

  5. Perception of change after treatment

    Time frame: 4-8 week

    By Patient Global Impression of Improvement (PGIC).

  6. Perception of Quality of life

    Time frame: 4-8 week

    By SF-8 scale. The SF-8 consists of 8 items comprising 8 dimensions (Bodily Pain, Perceptions, Mental Health, Physical Function, Role-physical, Role-emotional, Social Function, and Vitality).

    To assess each dimension, items are aggregated into a score ranging from 0 to 100; being higher scores indicators of good health.

  7. Trigger points pain

    Time frame: 4-8 week

    By algometer. Pressure was applied perpendicular to the skin, at a speed of 30kPa/s. Three measurements with 1 minute between measurements were averaged.

  8. Change in thorax position

    Time frame: 4-8 week

    Distance between acromion-bed.To assess the position of the upper trunk, the length of the pectoralis minor in the supine position is evaluated by measuring the distance between the posterior edge of the acromion and the stretcher while the patients remain in that position.

  9. Functional capacity

    Time frame: 4-8 week

    By Sit-to-stand test. Participants sit in a 43 cm tall armless chair (Fig. 1) as quickly as possible 5 times. Participants cross their arms over their chest and are instructed to fully stand up and make firm contact when sitting. Time begins with the "go" command and ends when participants sit down after the fifth stand-up.

  10. Frailty

    Time frame: 4-8 week

    By FRAIL Questionnaire. The FRAIL scale are short 5-question assessment of fatigue, resistance, aerobic capacity, illnesses, and loss of weight, classified the patients into 3 categories: robust (score = 0), prefrail (score = 1-2), and frail (score = 3-5).

  11. Motivation and self-efficacy

    Time frame: 4-8 week

    Participation motives are measured with the Exercise Motivation Index. The questionnaire consists of 15 statements followed by a five-point rating scale for each statement, ranging from 0 (not important) to 4 (extremely important). Although the authors found that the index was valid and reliable, they advise that further validation be made. Three subscores (0-4) were calculated by summing the scores for physical, psychological, and social motivation and dividing them by the number of statements for each area (Stenström, 1997; Klompstra, 2015) Cronbach's alpha was 0.889.

  12. Screening sarcopenia

    Time frame: 4-8 week

    Screening sarcopenia: SARC-F. There are 5 components of SARC-F questionnaire: strength, assistance with walking, rise from a chair, climb stairs, and fall. The SARC-F scores range from 0 to 10, with 0 to 2 points for each component. A score ≥4 is predictive of sarcopenia and poor outcomes.

Sponsors and collaborators

Lead sponsor

University of Valencia

Other

Registry information

Official study title

The Effect of Manual Therapy, Thera-band Exercise and Walking on Age-related Lung Function and Functional Capacity

Acronym: MTBEW

Important dates

Study start
2021
Primary completion
2022
Study completion
2023
First posted
Apr 14, 2020
Registry last updated
May 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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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