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To Check the effect of Alternate Therapy like BioFeedback on mental health of Individual in stress and Tension

Comparative Study of Biofeedback Therapies for Tension Type Headache Treatment and Enhancing Capacity towards Psychic Challenges

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/014895
Enrollment
240
Registered
2018-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: BioFeedback Therapy to patients distributed in 7 groups.: Frequency--They will be checked after 1, 3, 6 and 12 months for total duration of 1 year. The Duration for each therapy will b

Sponsors

ABESEC Ghaziabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects included in the study will be: 1-Subjects with headache fulfilling the criteria for TTH laid down by International Headache Society. 2-Both males and females between 18 to 65 years.

Exclusion criteria

Exclusion criteria: Subjects excluded from the study will be: 1-Subjects who underwent complementary alternative medicine interventions in the past 6 months. 2-Subjects with other headache types as described in International Classification of Headache Disorders (ICHD) - II classification. 3-Subjects with the presence of more than one type of headache in addition to tension type headache. 4-Subjects whose headache began after the age of 50 years. 5-Subjects with serious somatic or psychiatric disease. 6-Subjects with history of drug abuse or use of analgesics and triptans >10 days per month.

Design outcomes

Primary

MeasureTime frame
the primary variables selected for our study will be: -Average frequency of headache per week. -Average duration of headache per week. -Average intensity of headache per week. The recommendation for headache frequency reporting is consistent with the IHS guidelines for controlled trials of drug treatments100, 101 and will facilitate meta-analyses and other comparisons across studies of various interventions. Timepoint: The primary variables selected for our study will be calculated in: 1 month 3 months 6 months 12 months

Secondary

MeasureTime frame
The secondary variables considered in our study will be -SF-36 Quality of Life â?? total, physical and mental scores. -Analgesic consumption. These secondary variables are also termed as â??secondary non headache measuresâ?? by the American Headache Society Behavioral Clinical Trials Workgroup, 2005. Timepoint: Scorings will be recorded at 1 month 3 months 6 months 12 months

Countries

India

Contacts

Public ContactRohit Rastogi

Dayalbagh Educational Institute, Agra

dkc.foe@gmail.com9456433788

Outcome results

None listed

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