Clinical Trials Logo

Clinical Trial Summary

Impaired health related quality of life (HRQOL) including fatigue, problems with sleep and psychosocial well being (physical, emotional, and spiritual) have been noted in adult cancer survivors. Physical domain is one of the most common measured indicators of HRQOL. Despite the tremendous implications of having an impaired QOL, few studies have staged interventions aimed at improving HRQOL in a heterogeneous group of cancer survivors. There is little literature examining whether a yoga intervention is feasible in a heterogeneous group of cancer survivors.

The proposed research will utilize Vanderbilt Ingram Cancer Center (VICC), Nashville General Hospital (NGH) and REACH for Survivorship program for a pilot study. The investigators will see if a study using a broad range of diagnoses is feasible for a Yoga Intervention.


Clinical Trial Description

The Yoga Program

The yoga intervention will be developed by a certified yoga instructor. The yoga instructors teaching the classes will undergo training before teaching classes; all classes will embody the same positions and techniques. Based on Tantric Hatha yoga techniques, the intervention will incorporate physical stretches and poses, breathing exercises and meditation. All exercises will be done in a seated or reclined position. Yoga positions will focus on breathing exercises and basic stretching and will be at the easy or basic level. Yoga positions to be utilized in the intervention are located in the Appendix. Classes will include instruction on practicing the techniques taught in the classes at home.

The yoga instructors utilized in this study are certified in yoga instruction. The classes will be held over a period of 60 minutes in a quiet, dimly lit conference room at Gilda's Club and at Nashville General Hospital. The classes will combine physical postures (asanas), breathing (pranayama) and deep relaxation (savsana). It will be made clear that participants should not practice any pose that causes or exacerbates any discomfort. Yoga poses will be modified based on participants needs. Individual poses will be held from 20 seconds to 5 minutes depending on the poses. Classes will begin slowly and progress; adding poses to the same sequence, breath techniques and restorative poses for each class over the 10 weeks. Modifications and pose variations will be used to make the class appropriate for each individual. Chairs, yoga props, and a wall will be used to assist in poses. The class will consist of the following outline:

5 Minutes: Centering, Relaxation, Body Scan

- Seated (Sukasana, Simple Cross Legged Pose)

- Reclined (Savasana, Relaxation Pose)

10 minutes: Breathing techniques

- Diaphramic breathing (belly breath)

- Ujjayi breathing (builds heat and is an audible breath)

- Kapalabhati breathing (pumping breath)

- Nadi Sodhana breathing (alternate nostril breath)

10 minutes: Warming spine and body

- Cat/Cow

- Twists

- 1/2 Sun Salutations and variations

15 minutes: Strength building and stretching poses

- Hamstring Opener (reclined)

- Downward Dog (at wall or on floor)

- Lunges (at wall, with chair or with no props)

- Bridge Pose

- Locust Pose (with variations)

5 minutes: Restorative Poses

- Supported Bridge Pose

- Supported Child's Pose

- Supported Forward Twist

- Legs up Wall

- (rotate restorative poses throughout 10 weeks)

5 minutes:

- Savasana (final relaxation)

5 minutes:

- Mindfulness Meditation

More details about the positions are located in the Appendix.

Study Instruments

Short Form 36 (MOS SF-36): The MOS SF-36 contains eight individual scales from which we will generate the Physical Component (PCS) and the Mental Component Summary (MCS) scores. The eight scales include physical functioning, role function-physical, bodily pain, social functioning, mental health, role function-emotional, vitality and general health perceptions [33]. The MOS SF 36 has been validated in the general population and population norms have been established for comparison between specific groups. Each scale is scored from 0-100, with 100 being the most favorable score. The SF-36 has been validated in the general population and population norms have been established for comparison between specific groups. The summary scales have been standardized to a reference normal healthy population, with a mean score of 50 and deviation of 10 points. Within the SF-36 is a 4 item Vitality scale which can be used to determine the presence or absence of fatigue.

Brief Symptom Inventory-The BSI is a short 53 item instrument designed to measure three dimensions of psychological distress - somatization, depression and anxiety. Raw scores are converted to T scores on the basis of normative data. The T scores are then dichotomized, in which a T score 63 classified a respondent as having psychological distress.

Survivor Questionnaire: A self-report questionnaire will be used to ascertain all demographic and historical information on race, age, income, education, current and past employment status, and current and past marital status. Current medical conditions will be selected by the participant from checklist including major medical conditions including secondary malignancy, cardiac, pulmonary and thyroid dysfunction. In addition, participants will be asked to list their current medications such as thyroid replacement, immunosuppressants, and anti-depressants. Lifetime smoking and alcohol habits will also be quantified, as well as reproductive history. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01228955
Study type Observational
Source Vanderbilt University Medical Center
Contact
Status Completed
Phase N/A
Start date February 2010
Completion date March 2012

See also
  Status Clinical Trial Phase
Recruiting NCT06028048 - Enhancing Work Participation of Unemployed and Work-Disabled Cancer Survivors Phase 2/Phase 3
Recruiting NCT04439461 - Adaptation and First Step Validation of the ICF Core Set for Vocational Rehabilitation for Cancer Survivors
Completed NCT04498130 - Feasibility of a Novel, Theory Based Physical Activity Intervention Among Adult Cancer Survivors N/A
Completed NCT05473026 - Grateful Strides Toward Physical Activity and Well-Being for Black Breast Cancer Survivors N/A
Active, not recruiting NCT05582889 - Move For Your Health for Older Cancer Survivors N/A
Active, not recruiting NCT04339959 - Remote Assessment of Physical Function
Recruiting NCT05193149 - Inspiratory Muscle Training in Obese Breast Cancer Survivors N/A
Recruiting NCT03750981 - C.A.P.A.B.L.E. (Cross-Training and Physical Activity: A Better Life Experience Study) N/A
Completed NCT04751305 - Remote Exercise Maintenance With Health Coaching for Cancer Survivors N/A
Completed NCT02152020 - Patient-Centered Acupuncture for Pain (PCAP) N/A
Recruiting NCT05865678 - Musculoskeletal Health in Adult Haematological Cancer Survivors
Recruiting NCT06046573 - Pilot Study of Internet-Delivered Psychological Treatment for Cancer Survivors N/A
Recruiting NCT05194397 - Exercise Training and NR Supplementation Trial to Improve Fitness in AYA HCT Survivors Phase 2
Completed NCT01108484 - Program of Exercise, Diet and Control of Psychological Stress in Cancer Survivors N/A
Recruiting NCT06205251 - Diaphragm Structure and Function in Childhood Cancer Survivors N/A
Completed NCT03459781 - Compassion Meditation for Cancer Survivor-Caregiver Dyads Phase 1/Phase 2
Recruiting NCT05519982 - Sleep Treatment Education Program-1 (STEP-1) N/A
Completed NCT03981809 - Screening Tool to Identify the Dominant Pain Mechanism in Cancer Survivors: PainsCan
Active, not recruiting NCT04245943 - Rehabilitation - Physical Activity and Coping N/A
Active, not recruiting NCT04855552 - Telehealth Weight Loss Program for Breast Cancer Survivors N/A