Yoga for Stress and Mental Health

Not Applicable

Completed

• Conditions: Psychological Distress; Anxiety; Physiological Stress; Depression
• Interventions: Behavioral: Hatha Yoga

• Registration Number: NCT01652807
• Lead Sponsor: Southern Methodist University

Brief Summary

This study looks at an 8-week hatha yoga intervention for women reporting high levels of stress, a risk factor for various forms of psychopathology.

Detailed Description

Yoga practice appears to reduce stress and associated emotions. Specifically, yoga has been associated with significant decreases in depression, anxiety, and perceived stress. These findings underscore the promise of yoga practice for improving mental health in women prone to stress.

This study aims to examine the feasibility, acceptability, and efficacy of an eight-week Hatha Yoga intervention for improving stress and mental health. To this end, the investigators will recruit 40 women high in stress to receive an 8-week hatha yoga intervention consisting of two weekly 90-minute sessions. At baseline and at post-intervention, participants will undergo several cognitive, emotional, and behavioral assessments, followed by a relaxation time. Primary feasibility outcomes will be the time required to recruit 40 participants, the number of screen failures, participant retention and participant adherence to the study protocol. Acceptability will be evaluated with questionnaires and an interview during the final visit. Primary efficacy outcomes will be group differences in pre- to post-intervention change in perceived stress and various mental health parameters.

Study Timeline

• Study Start: 2012-02
• Study First Submitted: 2012-07-23
• Study First Submitted QC: 2012-07-25
• Study First Posted: 2012-07-30
• Primary Completion: 2013-09
• Study Completion: 2013-09
• Status Verified: 2015-01
• Last Update Submitted: 2015-01-12
• Last Update Posted: 2015-01-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 52

Inclusion Criteria

• Female patients between the ages of 25 and 45. We only will only include women in this age range due to age-related variations in estrogen levels that effect HPA reactivity in women (Seeman, Singer, Wilkinson & McEwen, 2001).
• Sedentary as defined by moderate-intensity exercise less than 60 minutes per week (this definition is consistent with that employed in previous studies of exercise interventions; e.g., Dunn et al., 2005; Trivedi et al., 2006). This criterion was selected in order to be able to test the effects of the yoga intervention.
• Written physician approval/medical clearance to participate in an exercise/yoga protocol.
• Capable and willing to give written informed consent, to understand inclusion and exclusion criteria.

Exclusion Criteria

• Have practiced yoga or engaged in other mind-body practices (e.g., tai chi, meditation) regularly (i.e., once a week or more) within the last year.
• Lifetime history of psychotic disorders of any type, bipolar disorder (I, II, or NOS), schizophrenia or schizoaffective disorder, or anorexia nervosa.
• Current alcohol or drug dependence.
• Screening BDI ≥ 30 (severe depression).
• Known or suspected to have significant personality dysfunction that could, in the investigator's opinion, interfere with trial participation.
• Currently at risk of self-harm or harm to others, in the Sponsor's opinion, based on clinical interview.
• Currently a psychiatric inpatient; have been hospitalized for a psychiatric condition within the past year.
• Have ever been diagnosed with organic brain syndrome, mental retardation, or other cognitive dysfunction that could interfere with their capacity to participate in the study protocol.
• Body mass index ≥ 40 (in order to screen out individuals with Class III obesity who might be more prone to musculoskeletal injuries than individuals with a BMI < 40.0) or < 18.5 (in order to screen out individuals whose hormone levels may be impacted by their low weight).
• Resting blood pressure ≥ 160 systolic and/or 100 diastolic. Individuals currently being treated for high blood pressure and meeting these criteria are eligible.
• Receiving concurrent psychotherapy of any kind.
• Use of any psychotropic medications.
• Positive result on pregnancy test at Screening; plan to become pregnant during the course of the trial.
• Insufficient command of the English language (i.e., they cannot carry on a conversation with an interviewer in the English language or read associated text).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Yoga	Hatha Yoga	The yoga intervention will last eight weeks and include two 90-minute sessions each week. Each yoga session will consist of the same series of 26 Hatha yoga postures, two breathing exercise, and two savasanas (i.e., a resting/relaxation posture), in a room heated to 104 degrees Fahrenheit, which aids in safe muscle stretching.

Primary Outcome Measures

Name	Time	Method
Perceived Stress Questionnaire	Weeks 0 (baseline) to 9 (post-intervention)	The PSQ (Levenstein et al., 1993) is a self- report measure of cognitive and emotional reactions to perceived stressful situations. The questionnaire consists of four subscales assessing (1) worries, anxious concern for the future, feelings of desperation and frustration; (2) tension, exhaustion, and lack of relaxation; (3) positive feelings of challenge, joy, energy, and security; and (4) perceived environmental demands, such as lack of time, pressure, and overload.

Secondary Outcome Measures

Name	Time	Method
Distress Tolerance	Weeks 0 (baseline) to 9 (post-intervention)	The DTS (Simons \& Gaher, 2005) is a 15-item self- report measure of physical and psychological distress tolerance.
Feasibility	Weeks 0 (baseline) to 9 (post-intervention)	Feasibility and acceptability of a yoga intervention for stress-induced eating. This interview, constructed by the PI, assesses participants' perceptions of ease of participation, program likeability, and perceived benefits of the yoga program. The interview consists of 16 open-ended questions.

Trial Locations

Locations (1)

Southern Methodist University; 🇺🇸 Dallas, Texas, United States