Healing Touch Prior to Cardiac Rehab

July 19, 2017 updated by: Scripps Health

Healing Touch Intervention in Post-Cardiac Event Patients Prior to Starting a Cardiac Rehab Program

The purpose of the investigators proposed randomized, controlled study is to examine the effect of 6 one hour treatments of Healing Touch (HT) over 3 weeks on post-cardiac event patients, while they wait to enter a Cardiac Rehab (CR) program.Patients enrolled in the Scripps Center for Integrative Medicine (SCIM) Cardiac Rehab Program typically experience a waiting period of 3 weeks, or sometimes more, before starting the program.

Secondary aims of the proposed study are to evaluate the effect of HT on CR program outcome measures of METs, BMI, physical and mental well-being, and attendance in this population.

New participants in the CR program who qualify and agree to participate in the study will be consented and randomly assigned to the Intervention Group who will receive Healing Touch therapy, or to the Control Group, which will not receive HT.

At baseline both groups will complete the Dartmouth Quality of Life and SF-36 Health Surveys. The questionnaires will be repeated at the end of the 3 week study period and at the end of the 3 months SCIM CR program.

An effect size of 15% was chosen, with an alpha level of 0.05, 80% power, 95% confidence level, and using a two-tailed test, it was determined that a sample size of 56 patients in each group would be needed for between group comparisons. To account for potential attrition the study will enroll 124 subjects, 62 in each group.

Our rationale is that Healing Touch, in addition to standard medical care will reduce post-cardiac event stress and anxiety symptoms in patients waiting to enter a cardiac rehab program, as measured by the Dartmouth Quality of Life Index and the SF36 questionnaire. Further, the investigators suggest that Healing Touch treatments will improve patient's final outcomes of the 12 week CR program.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Study Plan

HEALING TOUCH Healing Touch (HT) is an energy based approach to health and healing. It uses light touch to influence the energy field that surrounds the body, and energy centers which control the flow of energy to the physical body. HT can restore harmony and balance, which can affect all physical, mental, emotional, and spiritual health, as well as self-healing. HT complements traditional health care and is used together with other approaches to health and healing.

Healing touch has been studied for use in pain, cancer, endocrine-immune-HIV, mental health, and cardiovascular factors in patients ranging from pediatric to the elderly.

POST-CARDIAC EVENT STRESS AND ANXIETY SYMPTOMS Having a major cardiac event can be a stressful, life changing occurrence. Often, the psychological impacts of having a heart attack (myocardial infarction) are underestimated and can be long lasting. In fact, there is evidence to suggest that the emotional stressors that occur post-MI are consistent with symptoms of post-traumatic stress disorder (PTSD), which has been shown to be associated with higher rates of recurrent coronary events and overall increased mortality in diagnosed patients.

Studies have shown that mental stress has a negative effect on a person's heart health. In particular:

  • Unmanaged stress can lead to high blood pressure, arterial damage, irregular heart rhythms and a weakened immune system.
  • Patients with depression have been shown to have increased platelet reactivity, decreased heart variability and increased pro-inflammatory markers (such as C-reactive protein or CRP), which are all risk factors for cardiovascular disease.
  • For people with heart disease, depression can increase the risk of an adverse cardiac event such as a heart attack or blood clots. For people who do not have heart disease, depression can also increase the risk of a heart attack and development of coronary artery disease.
  • In one landmark study, the continued presence of depression after recovery increased the risk of death (mortality) to 17 percent within 6 months after a heart attack (versus 3 percent mortality in heart attack patients who didn't have depression). Frasure-Smith N, et al. Depression following myocardial infarction: Impact on 6-month survival. JAMA, October 20, 1993. 270(15):1819-1825.

RELATED STUDIES

HEALING TOUCH has been in use at Scripps hospitals since 1993. The Cardiac Healing Touch Program at the Scripps Center for Integrative Medicine at Scripps Clinic and Scripps Green Hospital collected data on 305 cardiac surgery patients. Unpublished outcomes revealed that post-surgical cardiac patients experienced a 74% reduction in pain and a 71% reduction in anxiety after receiving HT.

In another study performed by the Scripps Center for Integrative Medicine at a Marine Base near San Diego, called Complementary Medicine for PTSD and Related Symptoms in Returning Active Duty Military, revealed statistically and clinically significant reduction in PTSD (p <.0005, Cohen's d = .85), as well as depression (p <.0005, Cohen's d = .70) for the healing touch and guided imagery intervention versus the control group.

Post-cardiac event patients who have been referred to a Cardiac Rehab program often find that they are being asked to wait before a position becomes available in the CR program. In some programs this may involve a waiting period of several weeks. At the Scripps Center for Integrative Medicine Cardia Rehab program the waiting period is typically 3 weeks, or slighly more. During this period, many patients find that their stress and anxiety levels in reaction to their recent cardiac event remain untreated. It is this group of patients the investigators aim to enroll into the research study to determine whether 6 healing touch treatments during a waiting period of 3 weeks will decrease their stress and anxiety before entering the cardiac rehab program. Moreover, the investigators will follow the patients through CR and determine whether the pre-program HT treatments improve the patient's overall physical outcomes measures.

Research Methods

Baseline Assessment Upon enrollment in the study, including signing the consent, participants will answer questionnaires to assess their baseline status including demographics, brief medical history, and the following two questionnaires: Dartmouth Quality of Life and SF-36 Health Survey.

Randomization Following initial assessment, participants will be randomly assigned to the Intervention Group who will receive Healing Touch therapy, or to the Control Group, which will not receive HT. All study participants will enter the CR program after either 3 weeks of HT intervention or a 3 week waiting period. If there is no opening available immediately following the 3 week period, study subjects will be entered into the program as soon as a space is available.

Intervention Group

The HT group will receive two one hour sessions per week for a total of 6 sessions, over 3 weeks. Healing Touch practitioners who have completed the healing touch program and are certified healing touch practitioners will perform the healing touch sessions. Whenever possible each patient will be given the treatment by the same practitioner for all 6 sessions. The healing touch practitioner will center his/her-self by bringing mind, body, and emotions into a quiet and focused state of mind. They will then assess the patient's energy field and implement healing touch techniques in the following order:

Chakra Connection Chakra Connection is a full body technique to open, connect, and balance the major and minor chakras and help clear the energy field. It promotes relaxation, reduces pain and anxiety and promotes general well-being and prevention.

Mind Clearing This HT technique is helpful in promoting mental clarity, peace, and calm. It facilitates deep relaxation, clear thinking, and promotes healthy sleep.

Chakra Spread. Chakra Spread is a gentle energy technique designed to open the chakras and produce a deep healing. It is helpful during life transitions to promote a deep sense of calm and peace - physically, emotionally, mentally, and spiritually.

No other forms of healing will be administered by the HT practitioner. The HT practitioner will use light touch to implement the healing touch techniques. Healing touch sessions will last approximately one hour and will occur two times per week for three weeks for a total of 6 sessions.

To complete the study, patients must receive all 6 sessions. For potential scheduling conflicts, exceptions will be made to accommodate patients for a maximum of 4 weeks.

Post-Intervention Assessment After 3 weeks, all participants in both groups will complete the following questionnaires: Dartmouth Quality of Life Index and SF-36 Health Survey.

All patients will enter the CR program as soon as the CR staff can schedule each patient.

Control Group When subjects in this group have completed their CR program they are offered a complementary one-time, one hour, healing touch treatment.

Study Type

Interventional

Enrollment (Anticipated)

124

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • California
      • La Jolla, California, United States, 92037
        • Recruiting
        • Scripps Center for Integrative Medicine
        • Contact:
        • Contact:
        • Sub-Investigator:
          • Elizabeth Fraser, RN
        • Sub-Investigator:
          • Maureen Kowba, RN
        • Sub-Investigator:
          • Claire D'Andrea, RN

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 95 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Must have referral to Cardiac Rehab at the Scripps Center for Integrative Medicine.
  2. Must have had a cardiac event which precede the CR referral.
  3. Must be willing to come to the Scripps Center for Integrative Medicine twice a week for 3 weeks.
  4. Must be able to understand English

Exclusion Criteria:

  1. Patients under 18 years.
  2. Unable to understand English

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: SUPPORTIVE_CARE
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
OTHER: Intervention Group
This group will receive 6 Healing Touch treatments over 3 weeks
Healing Touch (HT) is an energy based approach to health and healing. It uses light touch to influence the energy field that surrounds the body, and energy centers which control the flow of energy to the physical body.
NO_INTERVENTION: Control Group[
This group will continue with their usual medical treatments but receive NO Healing Touch

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants with an improvement in stress and anxiety symptoms as measured by Dartmouth Quality of Life Index scores
Time Frame: 3 weeks
Dartmouth Quality of Life Index questionnaires will be obtained at enrollment and after 3 weeks of HT (or no intervention for the control group).
3 weeks
Number of participants with an improvement in stress and anxiety symptoms as measured by SF-36 scores
Time Frame: 3 weeks
SF-36 questionnaires will be obtained at enrollment and after 3 weeks of HT (or no intervention for the control group).
3 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants with an improvement of Metabolic Equivalent of Task (MET)
Time Frame: 3 months
MET: Metabolic Equivalent of Task is measured at the start of Cardiac Rehab and at 3 months completion.
3 months
Number of participants with an improvement in BMI: Body Mass Index
Time Frame: 3 months
BMI: Body Mass Index, which is measured at the start of Cardiac Rehab and at 3 months completion.
3 months
Number of participants with an improvement in stress and anxiety symptoms as measured by Dartmouth Quality of Life Index scores
Time Frame: 3 months
Dartmouth Quality of Life Index scores will be obtained at the start of cardiac rehab and at completion.
3 months
Number of cardiac rehab sessions each participant attended will be recorded
Time Frame: 3 months
To determine cardiac rehab attendance, study participants' number of sessions will be recorded. The program ends after 36 sessions (3 month). Not all participants complete all 36 sessions.
3 months
Number of participants with an improvement in stress and anxiety symptoms as measured by SF-36 scores
Time Frame: 3 months
SF-36 scores will be obtained at the start of cardiac rehab and at completion.
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Christopher Suhar, MD, Scripps Center for Integrative Medicine, Scripps Clinic

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2016

Primary Completion (ANTICIPATED)

December 1, 2018

Study Completion (ANTICIPATED)

June 1, 2019

Study Registration Dates

First Submitted

February 23, 2016

First Submitted That Met QC Criteria

February 25, 2016

First Posted (ESTIMATE)

March 1, 2016

Study Record Updates

Last Update Posted (ACTUAL)

July 21, 2017

Last Update Submitted That Met QC Criteria

July 19, 2017

Last Verified

July 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • IRB-16-6754

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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