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A study to find out effect of a Relaxation Exercise on Reducing Anxiety and Depression among Women with Breast and Reproductive organ Cancers in Goa

Effectiveness of a Relaxation Technique on Reducing Anxiety and Depression among Women with Breast Cancer in Goa: A Randomized Controlled Trial - READ

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/02/030996
Enrollment
60
Registered
2021-02-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: C50- Malignant neoplasm of breast Health Condition 2: C51-C58- Malignant neoplasms of female genital organs

Interventions

Intervention1: The intervention entails a 20 minutes relaxation session of Progressive Muscle Relaxation (PMR) with Deep Breathing and Guided Imagery (GI) sessions.: Progressive Muscle Relaxation (PM

Sponsors

Dr Dhanya Jose
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Adult women of age between 18 and 65 years with a new diagnosis of cancer, who have undergone surgery for Ca breast, Ca Cervix, Ca ovary, or Ca endometrium as their primary mode of treatment. 2)Those who are experiencing anxiety or depression (Zung anxiety scale score; SAA >44, Beck Depression Inventory; BDI >10, are not receiving medication for anxiety or depression. 3)Those who do not have cognitive impairment.

Exclusion criteria

Exclusion criteria: 1)Patients require medication for anxiety or depression during the study period. 2)Those who are not consenting to the study.

Design outcomes

Primary

MeasureTime frame
The primary outcome will be the difference between baseline and follow-up scores of anxiety, depression, and fatigue scales.Timepoint: Both groups will be assessed at baseline and the end of the two-week intervention period for their anxiety, depression and fatigue levels.

Secondary

MeasureTime frame
Secondary outcomes include the scores of anxiety, depression, and fatigue scales and the patients overall impression of the intervention. Timepoint: Both groups will be assessed at baseline and the end of the two-week intervention period for their anxiety, depression and fatigue levels. Patients feedback about the relaxation techniques will be collected at the end of the study.

Countries

India

Contacts

Public ContactDr Dhanya Jose

Goa Medical College

jkakodkar@hotmail.com9823928743

Outcome results

None listed

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