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OpenTrials
Completed

NCT Number: NCT06437756

Effects of Theraband Resistance Training on Muscle Strength in Coronary Artery Diseases

To compare the effects of Theraband Resistance Training with Conventional Resistance Training on muscle strength in coronary artery diseases

Completed

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Al Nafees Medical Hospital

Islamabad, Federal, 44000, Pakistan

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Participants having a documented diagnosis of CAD, confirmed by a medical professional.
  • Individuals with a history of myocardial infarction (heart attack), angina, or evidence of significant coronary artery stenosis.
  • Stable CAD who were not experiencing acute coronary events, such as recent heart attacks or unstable angina.
  • Patients who were able to perform exercises with TheraBand.
  • Reduced muscle strength of upper limb/lower limb

Exclusion criteria

  • Patients over the age of 75 years.
  • Exclude individuals with a recent history of Theraband resistance training.
  • Severe cardiovascular complications such as heart failure with reduced ejection fraction, severe arrhythmias, or uncontrolled hypertension.
  • Patients with unstable conditions or cardiac episodes.
  • Individuals who had undergone major cardiovascular surgery (e.g., coronary artery bypass grafting) within the last six months.
  • Ejection fraction < 40%

Treatment and study plan

Theraband resistance training

Other

Three sessions of 30 minutes each was used to complete the intervention over the course of six weeks (two sets of 12 repetitions). The participants were warmed up by stretching for 10 minutes before each session Participants were advised to take 5 mins rest before moving to next movement if they would feel fatigued after one movement. Thera-Band was utilized in only three different colors for the workouts.

Conventional Resistance Training

Other

The intervention was carried out over the course of six weeks in three sessions of 30 minutes each (two sets of 12 repetitions). The participants were warmed up by stretching for 10 minutes before each session. The resistance-training program was performed with Universal weights.

Primary outcomes

  1. Hand Held Dynamometer

    Time frame: 6 week

    If testing techniques are consistent, handheld dynamometry is a valid approach to assess the strength state and change in strength status. Hand-held dynamometry can be a reliable assessment technique when practiced by a single experienced tester

  2. Modified BORG Scale

    Time frame: 6 week

    The Modified Borg Dyspnea Scale is numerical rating scale ranging from 0 to 10 and is used to measure dyspnea that patient report during sub-maximal exercise and is regularly administered during six-minute walk test. Changes from the baseline will be measured

  3. Chadler Fatigue Scale

    Time frame: 6 week

    It is a self-administered questionnaire for assessing the degree and severity of fatigue/tiredness in epidemiological populations, both clinical and non-clinical. The Chadler Fatigue Scale (CFS) was originally perceived as comprising two subscales that evaluate fatigue in the physical and mental domains. Items are rated on a 4-point Likert scale (0 = better than usual, 1 = no more than usual, 2 = worse than usual, 3 = much worse than usual), with higher scores indicating greater fatigue. Changes from the baseline are measured

  4. 6 Min walk test (Distance in meters)

    Time frame: 6 week

    Changes from the baseline, Body Mass Index can be define as statistical index utilizing an individuals height and weight to give an estimation of muscle versus fat in female and male of all ages. It is determined by taking an individual weight in kilograms, separated by their height in meters squared, or BMI = weight (in kg)/height (in m square).

  5. The 30 Second Sit to Stand Test(30SSST) for lower limb strength

    Time frame: 6 week

    The 30-Second Sit to Stand Test evaluates older people's leg strength and endurance using a foldable chair without arms. Participants stand with feet positioned back from knees, arms crossed, and arms crossed. The examiner counts stand within 30 seconds, determining the score.

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
May 31, 2024
Registry last updated
Jul 3, 2024

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

View the official ClinicalTrials.gov record (opens in a new tab)

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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