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The effect of 12 weeks of continuous training and Interval training on oxidative stress and DNA damage in breast cancer survivors

The effect of 12 weeks of continuous training and Interval training on oxidative stress and DNA damage in breast cancer survivors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220418054577N1
Enrollment
45
Registered
2022-05-14
Start date
2022-08-22
Completion date
Unknown
Last updated
2022-08-29

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: Medium intensity continuous training: During the research, this group will perform three sessions of moderate intensity continuous training for 12 weeks and a week.

Sponsors

Private
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
54 Years to 60 Years

Inclusion criteria

Inclusion criteria: at least 6 months of complete discontinuation of breast cancer treatment permission of the physician to participating in the research women should be on the same levele in terms of health?life ? nutrition ?duration of illness body mass index shoul be above 25kg/m2.weight of body fat more than 30% ability to exercise with the approval of an oncologist and cardiologist menopause

Exclusion criteria

Exclusion criteria: Cardiovascular disease Diabetes disease Thyroid disease Smoking

Design outcomes

Primary

MeasureTime frame
Serum SOD levels. Timepoint: 48 hours before and after the desired interventions. Method of measurement: Blood sampling using ELISA method.;Serum GPX levels. Timepoint: 48 hours before and after the desired interventions. Method of measurement: Blood sampling using ELISA method.;Serum TAC levels. Timepoint: 48 hours before and after the desired interventions. Method of measurement: Blood sampling using ELISA method.;Serum MDA levels. Timepoint: 48 hours before and after the desired interventions. Method of measurement: Blood sampling using ELISA method.;Serum 8-OHdg levels. Timepoint: 48 hours before and after the desired interventions. Method of measurement: Blood sampling using ELISA method.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactparisa pournemati

Faculty of Physical Education and Sport Sciences - University of Tehran

p.pournemati@ut.ac.ir+98 21 8835 1730

Outcome results

None listed

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