Skip to content

Clinical trial on Effectiveness of Otago Exercise Training Programme on Multidimensional Fatigue Syndrome among Elderly Patients with Cancer

Clinical Trial on Effectiveness of Otago Exercise Training Programme on Multidimensional Fatigue Syndrome among Elderly Patients with Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121216285N3
Enrollment
82
Registered
2017-04-11
Start date
2017-03-05
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: Otago exercise is a training programme designed and conducted in University of Otago, New Zealand. The exercise will be implemented for 12 weeks, 5 days per week f
Rehabilitation
Intervention group: Otago exercise is a training programme designed and conducted in University of Otago, New Zealand. The exercise will be implemented for 12 weeks, 5 days per week for 40-60 minute
In subjects in intervention group Otago Exercise Programme will be implemented. In control group general health education will be given

Sponsors

Vice Chancellor for research; Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
60 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age 60 years old and above Being female MMSE more than 12 Having a care giver in ages range between 15 and 50 years old with health literacy Exclusion Criteria: The presence of acute cardiac, pulmonary, orthopedic or any disease which ban the subjects for doing exercises such as anemia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Multidimensional Fatigue Syndrom. Timepoint: Before intervention- After intervention. Method of measurement: Multidimensional Fatigue Inventory Syndrom.

Secondary

MeasureTime frame
Quality of Sleep. Timepoint: Before and After Intervention. Method of measurement: assessed by Sleep Quality Questionaire.;Neuromuscular pain. Timepoint: Before and after the intervention. Method of measurement: Using Pain Questionnaire.;Feeding problems and weight loss. Timepoint: Before and after the intervention. Method of measurement: Using BMI.;Stress. Timepoint: Before and after the intervention. Method of measurement: Using Stress Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Dadgari

Shahroud University of Medical Sciences

adadgri@yahoo.com+98 23 3239 4499

Outcome results

None listed

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