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Health benefits of exercise with acupressure for a cancer client

Effect of Multimodal intervention Vs Exercise programme on cancer related fatigue and quality of life among clients undergoing cancer treatment in selected hospitals at Mangaluru- Non randomized interventional trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/03/032017
Enrollment
200
Registered
2021-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: C509- Malignant neoplasm of breast of unspecified site

Interventions

Intervention1: Exercise program, Acupressure and Nutrition Education: Exercise program:10 exercises which will be taught to clients undergoing cancer treatment by demonstration and video clippings. On

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: � age between 18-65 years � both male and female patients who have undergone minimum of one cycle of cancer treatment � willing to participate in the study and attend all programs � with breast cancer, gynaecological cancer, head and neck cancers � those who are admitted in the hospital for minimum of 3 days

Exclusion criteria

Exclusion criteria: Cancer clients undergoing cancer treatment- � who are critically ill � already undergoing intensive (trainer-controlled optimized, twice a week, or more often) aerobic training � receiving erythropoietin or transfusions � having active infection, musculo skeletal problems, lower limb amputation � having neurological or cognitive disorders with functional deficits Cancer clients diagnosed with- � bone metastases, thrombocytopenia � uncontrolled hypertension, unstable angina, uncontrolled diabetes, cardiac insufficiency � lumbar disc osteoarthritis, peripheral arterial disease, chronic obstructive pulmonary disease and renal insufficiency � hypothyroidism or hyperthyroidism

Design outcomes

Primary

MeasureTime frame
Reduction in fatigue and quality of lifeTimepoint: before the intervention, after 21 days and after 3 months

Secondary

MeasureTime frame
haemoglobin level, platelet count, BMI and patient satisfactionTimepoint: before the intervention, after 21 days and after 3 months

Countries

India

Contacts

Public ContactSHAMBHAVI

Laxmi Memorial College Of Nursing

sunildsouza31@gmail.com9986012994

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026