Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Relaxation and stress-reduction using yoga or mindfulness for cancer survivors

Official title: Pilot Study of a Social/Behavioral Intervention on Cancer Survivors, Evaluating the Effect of Mind Body Interventions on Patient Reported Outcomes, Inflammation and Epigenetics.

Run by Stony Brook University · NCT07161713 · Data updated 2026-11-12

This study will test whether oncology-informed yoga or SMART mindfulness training can improve well-being and change epigenetic markers in adult survivors of lung, colon, and non-Hodgkin's lymphoma cancers.

More Cancer Survivors trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorStony Brook University
Academic / other
Drugs / interventionschemotherapy, immunotherapy
Locations1 site (Stony Brook, New York)
StatusRecruiting
StartedSeptember 17, 2025
Main results expectedSeptember 17, 2027
Study endsSeptember 30, 2027
Registry record updatedJuly 20, 2026
Trial IDNCT07161713 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are adults (18+) who survived lung, colon, or non-Hodgkin's lymphoma cancer, are at least six months post–cancer-directed treatment or off therapy, can provide saliva, and can complete English questionnaires.

Probably not a fit

Patients currently receiving active cancer treatment, those with primary anal or rectal cancers, pregnant individuals, those unable to produce saliva, or those who already practice yoga or SMART are unlikely to benefit or are ineligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a randomized interventional pilot trial assigning eligible adult survivors to oncology-informed yoga, SMART (Stress Management and Resiliency Training), or comparison to measure impacts on quality of life and symptom burden. Patient-reported outcomes will cover physical, social, emotional, and functional well-being, and saliva samples will be collected for exploratory epigenetic analysis. Enrollment is limited to adults at least six months after cancer-directed treatment or those off therapy who can provide saliva and complete questionnaires in English. The intervention is delivered at Stony Brook University Cancer Center with monitoring for adherence and safety.

Why it matters

Potential benefit: If successful, participants could experience improved physical and emotional quality of life and the study could reveal favorable changes in gene regulation related to stress.

How similar studies have gone: Previous trials have shown yoga and mindfulness improve quality of life in cancer survivors, but effects on epigenetic markers remain exploratory and less established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults over 18 years old
* Primary diagnosis: Lung Cancer, Colon Cancer and Non-Hodgkin's lymphoma (NHL)
* Six months post cancer-directed treatment (chemotherapy, targeted and immunotherapy). Patients with active disease (e.g. metastatic colorectal cancer) who are not receiving any cancer-directed treatment are eligible.
* Able to provide a saliva sample
* Gives informed consent and agrees to be randomly assigned
* Able to complete the questionnaire(s) in English.

Exclusion Criteria:

* Adults with primary anal and/or primary rectal cancer.
* Adult cancer survivors who are currently on an active treatment regimen.
* Oral or any pathological conditions that can limit the ability to produce saliva.
* Unable to participate in full length study period and follow up thereafter.
* Is pregnant or plan to become pregnant during the study period.
* Currently practicing yoga or SMART
* Those on corticosteroid therapy.
* Documented fall or syncope within the last 6 months

Where it's running

  • Stony Brook University Cancer Center
    Stony Brook, New York, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Need-based cancer survivorship program implementation

    This project tests a need-based survivorship program for adults who have finished cancer treatment to see if targeted screenings and referrals can help manage symptoms and weight concerns.

    Recruiting at 5 sites The University of Hong Kong · Hong Kong, Hong Kong and 4 other locations · NCT07830368

  • Brief Behavioral Activation for cancer survivors 65+

    This study tests whether a short behavioral-activation therapy delivered by phone or video can help reduce depression and anxiety and improve well-being in English- or Spanish-speaking cancer survivors aged 65 and older.

    Recruiting at 7 sites Memorial Sloan Kettering Cancer Center · Basking Ridge, New Jersey and 6 other locations · NCT07768449

  • Bridging psychosocial care after cancer treatment

    This study tests a routine digital distress screen plus a psycho-oncology navigation call to help cancer survivors access support after completing treatment.

    Recruiting University Hospital, Basel, Switzerland · Basel · NCT07672314

  • Hematologic cancer survivors after stem cell transplant try a personalized care plan

    This study tests a personalized Survivorship Care Plan for people with hematologic cancer who have undergone a stem cell transplant to see if it’s feasible within the Italian health system.

    Recruiting Azienda USL Reggio Emilia - IRCCS · Reggio Emilia · NCT07579065

  • Smartphone app to help follow the 2024 KDIGO chronic kidney disease guidelines

    This project will test whether a smartphone app helps young adults (ages 16–29) with chronic kidney disease follow the 2024 KDIGO guideline recommendations.

    Recruiting at 2 sites St. James's Hospital, Ireland · Dublin and 1 other locations · NCT07561957

  • Family-building support for young women after cancer

    This pilot tests whether a nurse-delivered four-session videoconference program helps young female cancer survivors make informed, values-based decisions about having children.

    Recruiting Duke University · Durham, North Carolina · NCT07471685

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.